SNP	p	logp	PMID	Study	Disease.Trait	survives_pruning_by_whole_catalog	survives_pruning_by_trait	survives_pruning_by_paper	survives_pruning_by_study
rs7910927	0E0	1000	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	1	1	1	1
rs8023580	0E0	1000	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	1	1	1	1
rs12498742	1E-700	700	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs4513773	1E-584	584	21757650	Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels.	Vascular endothelial growth factor levels	1	1	1	1
rs10490924	4E-540	539.397940008672	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	1	1	1	1
rs10737680	1E-434	434	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	1	1	1	1
rs3764261	7E-380	379.154901959986	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs6742078	5E-324	323.301029995664	19414484	Genome-wide association meta-analysis for total serum bilirubin levels.	Bilirubin levels	1	1	1	1
rs10490924	4E-322	321.397940008672	21665990	Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs2066938	4E-305	304.397940008672	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs7743761	5E-304	303.301029995664	20062062	Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.	Ankylosing spondylitis	1	1	1	1
rs2057681	1E-303	303	22982463	Clinical and genetic association of serum paraoxonase and arylesterase activities with cardiovascular risk.	Paraoxonase activity 	1	1	1	1
rs12913832	1E-300	300	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Eye color	1	1	1	1
rs12913832	1E-300	300	20463881	Digital quantification of human eye color highlights genetic association of three new loci.	Eye color traits	0	1	1	1
rs6910071	1E-299	299	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	1	1	1	1
rs2075650	1E-295	295	20460622	Genome-wide analysis of genetic loci associated with Alzheimer disease.	Alzheimer's disease	1	1	1	1
rs102275	4E-264	263.397940008672	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	1	1	1	1
rs1803274	6E-262	261.221848749616	21862451	GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors.	Butyrylcholinesterase levels	1	1	1	1
rs174547	8E-262	261.096910013008	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	0	1	1	1
rs1061170	1E-261	261	21665990	Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs13391552	5E-252	251.301029995664	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs13129697	2E-242	241.698970004336	20884846	Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.	Urate levels	0	0	1	1
rs1667394	1E-241	241	17952075	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Blue vs. brown eyes	0	1	1	1
rs964184	7E-240	239.154901959986	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	1	1	1	1
rs3135388	4E-225	224.397940008672	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	1	1	1	1
rs560887	9E-218	217.045757490561	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	1	1	1	1
rs10484554	4E-214	213.397940008672	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	1	1	1	1
rs2066847	6E-209	208.221848749616	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	NA	NA	NA	NA
rs3129889	1E-206	206	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs102275	1E-203	203	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	0	1	1	1
rs710446	2E-203	202.698970004336	22703881	Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.	Activated partial thromboplastin time	1	1	1	1
rs4349859	1E-200	200	21743469	Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.	Ankylosing spondylitis	1	1	1	1
rs867186	2E-200	199.698970004336	20802025	Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study.	Protein C levels	1	1	1	1
rs689	5E-196	195.301029995664	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	1	1	1	1
rs734553	1E-192	192	19503597	Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.	Uric acid levels	0	1	1	1
rs2274273	2E-188	187.698970004336	23056639	A genome-wide association study of circulating galectin-3.	Protein biomarker	1	1	1	1
rs2794520	2E-186	185.698970004336	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	1	1	1	1
rs5985	3E-186	185.52287874528	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	1	1	1	1
rs6457620	4E-186	185.397940008672	18794853	Common variants at CD40 and other loci confer risk of rheumatoid arthritis.	Rheumatoid arthritis	1	1	1	1
rs9271366	7E-184	183.154901959986	19525955	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.	Multiple sclerosis	0	0	1	1
rs37369	2E-182	181.698970004336	21572414	A genome-wide association study of metabolic traits in human urine.	Urinary metabolites	1	1	1	1
rs9923231	3E-181	180.52287874528	19300499	A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose.	Warfarin maintenance dose	1	1	1	1
rs174547	7E-179	178.154901959986	20037589	A genome-wide perspective of genetic variation in human metabolism.	Metabolite levels	0	0	1	1
rs12913832	1E-177	177	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Eye color	0	0	1	1
rs10830963	6E-175	174.221848749616	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	1	1	1	1
rs629301	1E-170	170	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	1	1	1	1
rs2981579	2E-170	169.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs16890979	7E-168	167.154901959986	18834626	Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study.	Urate levels	0	0	1	1
rs12913832	1E-167	167	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Hair color	0	1	0	0
rs11209026	8E-161	160.096910013008	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs12913832	1E-158	158	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Eye color	0	0	0	0
rs2075650	2E-157	156.698970004336	19734902	Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.	Alzheimer's disease	0	0	1	1
rs174547	4E-154	153.397940008672	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	1	1
rs102275	8E-153	152.096910013008	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs1535	3E-152	151.52287874528	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs174535	1E-151	151	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs4420638	8E-149	148.096910013008	22832961	Genome-wide association study of Alzheimer's disease.	Alzheimer's disease	0	0	1	1
rs4420638	9E-147	146.045757490561	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	1	1
rs1805007	2E-142	141.698970004336	17952075	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Red vs non-red hair color	1	1	1	1
rs3024321	8E-142	141.096910013008	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	0	0	0
rs4246215	1E-139	139	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs4420638	9E-139	138.045757490561	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	0	1	1	1
rs10490924	2E-138	137.698970004336	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (CNV)	0	1	1	1
rs911119	2E-138	137.698970004336	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs2231142	1E-134	134	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs9272346	5E-134	133.301029995664	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 1 diabetes	0	1	1	1
rs6927022	5E-133	132.301029995664	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	0	1	1	1
rs1260326	6E-133	132.221848749616	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	1	1	1	1
rs629301	6E-131	130.221848749616	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs9272346	6E-129	128.221848749616	18978792	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.	Type 1 diabetes	0	0	1	1
rs687289	1E-128	128	23267103	Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.	Coagulation factor levels	1	1	1	1
rs12203592	7E-127	126.154901959986	18483556	A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.	Black vs. blond hair color	1	1	1	1
rs1183910	2E-124	123.698970004336	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	1	1	1	1
rs579459	3E-123	122.52287874528	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alkaline phosphatase)	0	1	1	1
rs4253238	1E-122	122	23381795	Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1.	Circulating vasoactive peptide levels 	1	1	1	1
rs1799969	1E-120	120	21533024	Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci.	Soluble ICAM-1	1	1	1	1
rs1558902	5E-120	119.301029995664	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs10490924	5E-119	118.301029995664	20385826	Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).	Age-related macular degeneration	0	0	1	1
rs8070723	2E-118	117.698970004336	21685912	Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.	Progressive supranuclear palsy	1	1	1	1
rs6511720	4E-117	116.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	1	1	1	1
rs1061170	4E-117	116.397940008672	20385826	Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).	Age-related macular degeneration	0	0	1	1
rs854572	5E-116	115.301029995664	22982463	Clinical and genetic association of serum paraoxonase and arylesterase activities with cardiovascular risk.	Paraoxonase activity 	1	1	1	1
rs174547	9E-116	115.045757490561	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs12678919	2E-115	114.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	1	1	1	1
rs3803662	2E-114	113.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs1367117	4E-114	113.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	1	1	1	1
rs560887	2E-113	112.698970004336	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs9898	1E-111	111	22703881	Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.	Activated partial thromboplastin time	1	1	1	1
rs2476601	2E-111	110.698970004336	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	1	1	1	1
rs1410996	2E-111	110.698970004336	20385826	Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).	Age-related macular degeneration	0	0	0	0
rs4420638	5E-111	110.301029995664	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs8043757	5E-110	109.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs2073398	1E-109	109	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs7681423	1E-109	109	21757653	Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease.	Fibrinogen	1	1	1	1
rs2282679	2E-109	108.698970004336	20541252	Common genetic determinants of vitamin D insufficiency: a genome-wide association study.	Vitamin D insufficiency	1	1	1	1
rs9268853	5E-109	108.301029995664	21653640	Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways.	Rheumatoid arthritis	0	0	1	1
rs1061170	1E-108	108	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (CNV)	0	1	1	1
rs660895	1E-108	108	17804836	TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.	Rheumatoid arthritis	0	0	1	1
rs12150660	2E-106	105.698970004336	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	1	1	1	1
rs10830963	4E-105	104.397940008672	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs713598	2E-104	103.698970004336	20675712	The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12.	Bitter taste response	1	1	1	1
rs1532085	9E-104	103.045757490561	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	1	1	1	1
rs7961894	1E-103	103	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs12913832	4E-103	102.397940008672	18483556	A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.	Black vs. blond hair color	0	1	1	1
rs11603334	3E-102	101.52287874528	21873549	Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.	Proinsulin levels	1	1	1	1
rs11977526	3E-101	100.52287874528	21216879	A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3.	Insulin-like growth factors	1	1	1	1
rs9268645	1E-100	100	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs12191877	1E-100	100	19169254	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.	Psoriasis	0	0	1	1
rs687621	9E-100	99.0457574905607	22703881	Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.	Activated partial thromboplastin time	0	1	1	1
rs12678919	1E-97	97	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	0	0
rs6511720	7E-97	96.1549019599857	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs1805007	1E-96	96	17952075	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Freckles	0	1	0	0
rs1532085	3E-96	95.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	1	1
rs1367117	4E-96	95.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs2014355	5E-96	95.301029995664	20037589	A genome-wide perspective of genetic variation in human metabolism.	Metabolite levels	0	1	1	1
rs1532624	9E-94	93.0457574905607	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	HDL cholesterol	0	0	1	1
rs1800775	3E-93	92.5228787452803	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	1	1	1
rs1800775	4E-93	92.397940008672	20031564	Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study.	HDL cholesterol	0	0	1	1
rs2187668	8E-93	92.096910013008	21323541	Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy.	Nephropathy (idiopathic membranous)	1	1	1	1
rs1803274	6E-92	91.2218487496163	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	1	1	1
rs4607517	7E-92	91.1549019599857	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	1	1	1	1
rs4345897	2E-91	90.698970004336	23281178	A genome-wide assessment of variability in human serum metabolism.	Metabolite levels	1	1	1	1
rs2497938	2E-91	90.698970004336	22693459	Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.	Male-pattern baldness	NA	NA	NA	NA
rs12203592	2E-91	90.698970004336	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Freckling	0	1	1	1
rs507666	3E-91	90.5228787452803	21533024	Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci.	Soluble ICAM-1	0	1	1	1
rs3130544	2E-90	89.698970004336	23055271	Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.	Myasthenia gravis 	1	1	1	1
rs6050	9E-90	89.0457574905607	21757653	Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease.	Fibrinogen	0	0	0	0
rs429608	4E-89	88.397940008672	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	1	1	1	1
rs5498	6E-89	88.2218487496164	21533024	Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci.	Soluble ICAM-1	0	0	0	0
rs157580	8E-89	88.096910013008	21627779	The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease.	Alzheimer's disease	1	1	1	1
rs10501320	1E-88	88	21873549	Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.	Proinsulin levels	1	1	1	1
rs2545801	6E-88	87.2218487496164	22703881	Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.	Activated partial thromboplastin time	1	1	1	1
rs12913832	9E-88	87.0457574905607	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Hair color	0	0	0	0
rs12931267	5E-87	86.301029995664	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Hair color	0	1	1	1
rs1800775	5E-87	86.301029995664	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs724016	3E-86	85.5228787452803	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs4895441	7E-86	85.1549019599857	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	1	1	1	1
rs2476601	9E-85	84.0457574905607	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs12143842	1E-83	83	19587794	Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.	QT interval	1	1	1	1
rs11742570	2E-82	81.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs651007	2E-82	81.698970004336	20147318	Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes.	E-selectin levels	0	1	1	1
rs1800775	1E-81	81	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs1558902	2E-81	80.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs3135388	9E-81	80.0457574905607	17660530	Risk alleles for multiple sclerosis identified by a genomewide study.	Multiple sclerosis	0	0	1	1
rs2476601	2E-80	79.698970004336	17554260	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.	Type 1 diabetes	0	0	1	1
rs12150660	4E-80	79.397940008672	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	0	0	0
rs2420371	4E-80	79.397940008672	22443383	Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs7185735	1E-79	79	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs1057910	3E-79	78.5228787452803	19300499	A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose.	Warfarin maintenance dose	1	1	1	1
rs12143842	2E-78	77.698970004336	19305408	Common variants at ten loci influence QT interval duration in the QTGEN Study.	QT interval	0	0	1	1
rs12143842	2E-78	77.698970004336	19305409	Common variants at ten loci modulate the QT interval duration in the QTSCD Study.	QT interval	0	0	1	1
rs1800775	8E-78	77.096910013008	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs12913832	1E-77	77	18483556	A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.	Black vs. red hair color	0	1	0	0
rs10737680	2E-76	75.698970004336	20385819	Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs2981582	2E-76	75.698970004336	17529967	Genome-wide association study identifies novel breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs35853021	7E-76	75.1549019599857	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	0	1	1	1
rs7270101	9E-76	75.0457574905607	20173735	ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C.	Chronic Hepatitis C infection	1	1	1	1
rs173539	4E-75	74.397940008672	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	HDL cholesterol	0	0	1	1
rs6457617	5E-75	74.301029995664	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Rheumatoid arthritis	0	0	0	0
rs11710456	6E-75	74.2218487496163	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6817105	2E-74	73.698970004336	22544366	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	Atrial fibrillation	1	1	1	1
rs6800541	2E-74	73.698970004336	20062060	Genome-wide association study of PR interval.	PR interval	1	1	1	1
rs887829	3E-74	73.5228787452803	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs2476601	9E-74	73.0457574905607	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs16991615	1E-73	73	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs1800775	1E-73	73	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	HDL cholesterol	0	0	1	1
rs1051730	3E-73	72.5228787452803	20418890	Genome-wide meta-analyses identify multiple loci associated with smoking behavior.	Smoking behavior	1	1	1	1
rs13191343	2E-72	71.698970004336	20953186	Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis.	Psoriatic arthritis	0	1	1	1
rs10490924	3E-72	71.5228787452803	22694956	Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.	Age-related macular degeneration	0	0	1	1
rs3117242	1E-71	71	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	1	1	1	1
rs211718	2E-71	70.698970004336	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs7671266	9E-71	70.0457574905607	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	1	1	1
rs173539	3E-70	69.5228787452803	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	1	1	1
rs7442295	3E-70	69.5228787452803	18327256	SLC2A9 influences uric acid concentrations with pronounced sex-specific effects.	Urate levels	0	0	1	1
rs12994997	4E-70	69.397940008672	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs1165151	7E-70	69.1549019599857	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs855791	1E-69	69	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs887829	1E-69	69	19419973	Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.	Bilirubin levels	0	0	1	1
rs1051730	2E-69	68.698970004336	20418888	Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior.	Smoking behavior	0	0	1	1
rs1354034	3E-69	68.5228787452803	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs2076756	4E-69	68.397940008672	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	1	1	1	1
rs7776054	7E-69	68.1549019599857	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular hemoglobin	0	1	0	0
rs6426833	2E-68	67.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	1	1	1	1
rs2731672	1E-67	67	23381795	Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1.	Circulating vasoactive peptide levels 	0	1	1	1
rs1408272	5E-67	66.301029995664	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs1061170	5E-67	66.301029995664	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (GA)	0	1	0	0
rs1532624	1E-66	66	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs1051730	2E-66	65.698970004336	20418889	Meta-analysis and imputation refines the association of 15q25 with smoking quantity.	Smoking behavior	0	0	1	1
rs560887	2E-66	65.698970004336	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	0	0	0
rs7157785	9E-66	65.0457574905607	19798445	Genetic determinants of circulating sphingolipid concentrations in European populations.	Sphingolipid levels	1	1	1	1
rs1805007	1E-65	65	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Tanning	0	1	1	1
rs1351394	2E-65	64.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs173539	3E-65	64.5228787452803	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	1	1	1
rs356219	6E-65	64.2218487496164	22438815	Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.	Parkinson's disease	1	1	1	1
rs11209026	1E-64	64	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs174547	3E-64	63.5228787452803	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs1329428	3E-64	63.5228787452803	20861866	Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs676210	4E-64	63.397940008672	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	1	1	1
rs102275	7E-64	63.1549019599857	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs174536	1E-63	63	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs211718	1E-63	63	20037589	A genome-wide perspective of genetic variation in human metabolism.	Metabolite levels	0	1	1	1
rs614367	2E-63	62.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs1535	3E-63	62.5228787452803	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs17042171	4E-63	62.397940008672	19597492	Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.	Atrial fibrillation	0	0	1	1
rs11465804	7E-63	62.1549019599857	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs4420065	4E-62	61.397940008672	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	1	1	1	1
rs964184	4E-62	61.397940008672	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	Triglycerides	0	0	1	1
rs4148325	5E-62	61.301029995664	21646302	Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels.	Bilirubin levels	0	0	1	1
rs12931267	8E-62	61.096910013008	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Freckling	0	1	0	0
rs6136	4E-61	60.397940008672	20167578	Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels.	Soluble levels of adhesion molecules	1	1	1	1
rs10490924	1E-60	60	20861866	Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs4420638	1E-60	60	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	LDL cholesterol	0	0	1	1
rs174448	3E-60	59.5228787452803	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs2286963	3E-60	59.5228787452803	20037589	A genome-wide perspective of genetic variation in human metabolism.	Metabolite levels	1	1	1	1
rs2231142	3E-60	59.5228787452803	18834626	Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study.	Urate levels	0	0	1	1
rs3793917	4E-60	59.397940008672	20385819	Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs7759938	5E-60	59.301029995664	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs247617	9E-60	59.0457574905607	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs4246215	9E-60	59.0457574905607	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs11668344	1E-59	59	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs6558295	2E-59	58.698970004336	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs1800775	2E-59	58.698970004336	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs2000999	8E-59	58.096910013008	22403646	A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels.	Haptoglobin levels	1	1	1	1
rs17145738	9E-59	58.0457574905607	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	1	1	1	1
rs143384	1E-58	58	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs6795970	1E-58	58	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	1	1	1
rs1127354	2E-58	57.698970004336	20173735	ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C.	Chronic Hepatitis C infection	1	1	1	1
rs7412	3E-58	57.5228787452803	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	0	1	1	1
rs174538	5E-58	57.301029995664	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs174535	6E-58	57.2218487496163	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs1333049	7E-58	57.1549019599857	21606135	A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.	Coronary heart disease	1	1	1	1
rs174550	1E-57	57	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs560887	1E-57	57	19060907	Variants in MTNR1B influence fasting glucose levels.	Fasting plasma glucose	0	1	1	1
rs13387042	2E-57	56.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs4129267	2E-57	56.698970004336	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs3764261	2E-57	56.698970004336	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs17101394	3E-57	56.5228787452803	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Sphingolipid levels	0	0	1	1
rs603424	3E-57	56.5228787452803	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs505922	5E-57	56.301029995664	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	1	1	1
rs964184	6E-57	56.2218487496163	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs342293	7E-57	56.1549019599857	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs445925	1E-56	56	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity and mass	0	1	1	1
rs10781499	4E-56	55.397940008672	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs561241	4E-56	55.397940008672	22703881	Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.	Prothrombin time	1	1	1	1
rs4607517	8E-56	55.096910013008	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs676210	9E-56	55.0457574905607	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs9268853	1E-55	55	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	0	1	1
rs12150660	2E-55	54.698970004336	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	0	0	0
rs1805007	2E-55	54.698970004336	17952075	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Skin sensitivity to sun	0	1	0	0
rs2954029	3E-55	54.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	1	1	1	1
rs1532624	3E-55	54.5228787452803	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs174574	4E-55	54.397940008672	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs4246215	6E-55	54.2218487496163	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs4409764	1E-54	54	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs1354034	3E-54	53.5228787452803	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	0	0
rs9275390	3E-54	53.5228787452803	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	1	1	1
rs16926246	3E-54	53.5228787452803	20858683	Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.	Glycated hemoglobin levels	1	1	1	1
rs1800775	1E-53	53	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs646776	2E-53	52.698970004336	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	1	1	1
rs1667394	2E-53	52.698970004336	17952075	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Blue vs. green eyes	0	1	0	0
rs4638289	3E-53	52.5228787452803	21124955	Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A.	Amyloid A Levels	1	1	1	1
rs780094	6E-53	52.2218487496164	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs2188962	1E-52	52	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs687621	2E-52	51.698970004336	23650146	A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Venous thromboembolism	0	1	1	1
rs4698036	2E-52	51.698970004336	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	0	0	0
rs4971516	2E-52	51.698970004336	21059979	Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish.	LDL cholesterol	1	1	1	1
rs3131379	2E-52	51.698970004336	18204446	Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.	Systemic lupus erythematosus	1	1	1	1
rs12913832	3E-52	51.5228787452803	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Eye color	0	0	0	0
rs4253238	4E-52	51.397940008672	23381795	Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1.	Circulating vasoactive peptide levels 	0	0	0	0
rs12029080	6E-52	51.2218487496163	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	1	1	1	1
rs11075990	2E-51	50.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Body mass index	0	0	0	0
rs4353250	2E-51	50.698970004336	21124955	Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A.	Amyloid A Levels	0	0	0	0
rs7903146	2E-51	50.698970004336	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	1	1	1	1
rs1051730	2E-51	50.698970004336	19836008	A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.	Lung adenocarcinoma	0	1	1	1
rs6511720	2E-51	50.698970004336	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	LDL cholesterol	0	0	1	1
rs4803750	3E-51	50.5228787452803	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	1	1
rs6427196	4E-51	50.397940008672	23650146	A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Venous thromboembolism	0	1	1	1
rs12075	4E-51	50.397940008672	22291609	A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.	Inflammatory biomarkers	1	1	1	1
rs9939609	4E-51	50.397940008672	19079261	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.	Body mass index	0	0	1	1
rs7689420	6E-51	50.2218487496163	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2187668	1E-50	50	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs995030	2E-50	49.698970004336	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	1	1	1	1
rs1976403	2E-50	49.698970004336	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alkaline phosphatase)	1	1	1	1
rs4245791	2E-50	49.698970004336	20529992	Genetic regulation of serum phytosterol levels and risk of coronary artery disease.	Phytosterol levels	1	1	1	1
rs715	3E-50	49.5228787452803	23378610	Genetic variants associated with glycine metabolism and their role in insulin sensitivity and type 2 diabetes.	Metabolite levels	1	1	1	1
rs6903608	3E-50	49.5228787452803	21037568	A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).	Hodgkin's lymphoma	0	1	1	1
rs10830963	3E-50	49.5228787452803	19060907	Variants in MTNR1B influence fasting glucose levels.	Fasting plasma glucose	0	1	1	1
rs643434	1E-49	49	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	0	0	0
rs9938149	2E-49	48.698970004336	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs2282679	2E-49	48.698970004336	20418485	Genome-wide association study of circulating vitamin D levels.	Vitamin D levels	0	1	1	1
rs409801	3E-49	48.5228787452803	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs2300478	3E-49	48.5228787452803	21779176	Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.	Restless legs syndrome	1	1	1	1
rs2867125	3E-49	48.5228787452803	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs7241918	3E-49	48.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs6065906	3E-49	48.5228787452803	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	1	1	1	1
rs12896399	1E-48	48	17952075	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Blond vs. brown hair color	1	1	1	1
rs7901695	1E-48	48	17463249	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs4129267	2E-48	47.698970004336	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	0	1	1	1
rs7111341	4E-48	47.397940008672	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs2836878	5E-48	47.301029995664	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs1303	5E-48	47.301029995664	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	1	1	1	1
rs12051272	6E-48	47.2218487496163	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	1	1	1	1
rs7961894	7E-48	47.1549019599857	19110211	A genome-wide association study identifies three loci associated with mean platelet volume.	Mean platelet volume	0	0	1	1
rs3197999	1E-47	47	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs9483788	1E-47	47	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Other erythrocyte phenotypes	0	1	0	0
rs8050136	1E-47	47	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Body mass index	0	0	1	1
rs10665	2E-47	46.698970004336	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	1	1	1
rs10801555	2E-47	46.698970004336	22694956	Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.	Age-related macular degeneration	0	0	1	1
rs7412	2E-47	46.698970004336	22331829	Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial.	Response to statin therapy (LDL-C)	0	1	1	1
rs356219	2E-47	46.698970004336	21292315	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.	Parkinson's disease	0	0	1	1
rs4299376	2E-47	46.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	1	1
rs676210	3E-47	46.5228787452803	23247145	Genome-wide association study pinpoints a new functional apolipoprotein B variant influencing oxidized low-density lipoprotein levels but not cardiovascular events: AtheroRemo Consortium.	LDL (oxidized)	0	1	1	1
rs3811647	3E-47	46.5228787452803	21208937	Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.	Iron levels	1	1	1	1
rs1991431	4E-47	46.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs644234	4E-47	46.397940008672	23056639	A genome-wide association study of circulating galectin-3.	Protein biomarker	0	1	1	1
rs6754295	4E-47	46.397940008672	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs1799969	4E-47	46.397940008672	18604267	Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women.	Soluble ICAM-1	0	0	1	1
rs9399137	5E-47	46.301029995664	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs964184	5E-47	46.301029995664	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	0	0
rs10490924	7E-47	46.1549019599857	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (GA)	0	1	0	0
rs42235	8E-47	46.096910013008	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs12916	9E-47	46.0457574905607	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	1	1	1	1
rs2181540	1E-46	46	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	0	0	0
rs830124	1E-46	46	21572414	A genome-wide association study of metabolic traits in human urine.	Urinary metabolites	1	1	1	1
rs1800562	1E-46	46	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	0	1	1	1
rs6258	3E-46	45.5228787452803	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	1	1	1	1
rs17632542	3E-46	45.5228787452803	21160077	Genetic correction of PSA values using sequence variants associated with PSA levels.	Prostate-specific antigen levels	1	1	1	1
rs10761659	6E-46	45.2218487496164	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs6449353	7E-46	45.1549019599857	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs738409	1E-45	45	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alanine transaminase)	1	1	1	1
rs9272219	1E-45	45	21653640	Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways.	Rheumatoid arthritis	0	0	1	1
rs3118905	1E-45	45	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1042034	1E-45	45	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	0	0
rs6065906	1E-45	45	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs11710456	2E-45	44.698970004336	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6041	2E-45	44.698970004336	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	0	0	0
rs12029454	3E-45	44.5228787452803	19305408	Common variants at ten loci influence QT interval duration in the QTGEN Study.	QT interval	0	0	0	0
rs4299376	4E-45	44.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs365990	5E-45	44.301029995664	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs12916	5E-45	44.301029995664	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs7310409	7E-45	44.1549019599857	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	0	1	1	1
rs10758669	8E-45	44.0969100130081	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs1260326	1E-44	44	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs7075195	2E-44	43.698970004336	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	0	1	1	1
rs11591147	2E-44	43.698970004336	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	LDL cholesterol	1	1	1	1
rs4420638	2E-44	43.698970004336	17998437	Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease.	Alzheimer's disease	0	0	1	1
rs2191349	3E-44	43.5228787452803	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	1	1	1	1
rs7961894	3E-44	43.5228787452803	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	0	0	1	1
rs4977574	3E-44	43.5228787452803	19198609	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.	Myocardial infarction (early onset)	0	1	1	1
rs11710456	5E-44	43.301029995664	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs182052	5E-44	43.301029995664	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	1	1	1	1
rs6017342	1E-43	43	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	1	1	1	1
rs3734398	1E-43	43	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs916977	1E-43	43	18252221	Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene.	Iris color	0	1	1	1
rs10830963	3E-43	42.5228787452803	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	0	0	0
rs4420638	3E-43	42.5228787452803	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	LDL cholesterol	0	0	1	1
rs1049296	5E-43	42.301029995664	21665994	Genome-wide association study identifies two loci strongly affecting transferrin glycosylation.	Alcohol consumption (transferrin glycosylation)	0	1	1	1
rs2289252	6E-43	42.2218487496164	22703881	Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.	Activated partial thromboplastin time	0	1	1	1
rs10468017	7E-43	42.1549019599857	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	0	1	1	1
rs2131925	9E-43	42.0457574905607	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	1	1	1	1
rs6871626	1E-42	42	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs4810479	2E-42	41.698970004336	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	1	1	1
rs6810075	2E-42	41.698970004336	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	0	0	0
rs17646946	2E-42	41.698970004336	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs12740374	2E-42	41.698970004336	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	LDL cholesterol	0	0	1	1
rs673548	5E-42	41.301029995664	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs445925	6E-42	41.2218487496163	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	1	1	1
rs571312	6E-42	41.2218487496163	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs6679677	6E-42	41.2218487496163	18794853	Common variants at CD40 and other loci confer risk of rheumatoid arthritis.	Rheumatoid arthritis	0	0	1	1
rs3024505	7E-42	41.1549019599857	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs9402686	7E-42	41.1549019599857	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Hematological parameters	0	1	1	1
rs2230199	1E-41	41	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	1	1	1	1
rs12150660	1E-41	41	21998597	Genetic determinants of serum testosterone concentrations in men.	Testosterone levels	0	1	1	1
rs17366568	1E-41	41	20018283	Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals.	Adiponectin levels	1	1	1	1
rs734553	1E-41	41	19503597	Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.	Uric acid levels	0	0	0	0
rs579459	2E-41	40.698970004336	20167578	Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels.	Soluble levels of adhesion molecules	0	1	1	1
rs12678919	2E-41	40.698970004336	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	Triglycerides	0	0	1	1
rs2413450	3E-41	40.5228787452803	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	0	1	1	1
rs2200733	3E-41	40.5228787452803	17603472	Variants conferring risk of atrial fibrillation on chromosome 4q25.	Atrial fibrillation/atrial flutter	0	1	1	1
rs11160190	4E-41	40.397940008672	22907691	Genetic variation in the vaspin gene affects circulating serum vaspin concentrations.	Vaspin levels	1	1	1	1
rs800292	5E-41	40.301029995664	23620142	Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.	Circulating myeloperoxidase levels (serum) 	0	1	1	1
rs2131925	5E-41	40.301029995664	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs3792109	7E-41	40.1549019599857	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs157580	1E-40	40	19125160	Examination of the current top candidate genes for AD in a genome-wide association study.	Alzheimer's disease	0	0	1	1
rs6679677	1E-40	40	18978792	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.	Type 1 diabetes	0	0	1	1
rs9349204	2E-40	39.698970004336	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs7903146	2E-40	39.698970004336	22693455	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.	Type 2 diabetes	0	0	1	1
rs1495743	2E-40	39.698970004336	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs4971516	2E-40	39.698970004336	21059979	Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish.	LDL cholesterol	0	0	0	0
rs4420638	2E-40	39.698970004336	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	LDL cholesterol	0	0	1	1
rs6711012	3E-40	39.5228787452803	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs7652995	3E-40	39.5228787452803	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1464510	3E-40	39.5228787452803	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	1	1	1	1
rs6065904	4E-40	39.397940008672	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs1260326	5E-40	39.301029995664	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	0	1	1	1
rs505922	7E-40	39.1549019599857	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	1	1	1
rs17277546	9E-40	39.0457574905607	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs612169	9E-40	39.0457574905607	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs1884302	1E-39	39	23160099	A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.	Sagittal craniosynostosis	1	1	1	1
rs10738760	1E-39	39	21757650	Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels.	Vascular endothelial growth factor levels	1	1	1	1
rs1800788	1E-39	39	21757653	Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease.	Fibrinogen	0	0	0	0
rs806794	1E-39	39	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1532624	1E-39	39	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs6047844	2E-39	38.698970004336	22693459	Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.	Male-pattern baldness	1	1	1	1
rs10484554	2E-39	38.698970004336	18369459	A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci.	Psoriasis	0	0	1	1
rs218238	3E-39	38.5228787452803	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs646776	4E-39	38.397940008672	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs1408272	4E-39	38.397940008672	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular hemoglobin	0	1	0	0
rs10455872	5E-39	38.301029995664	21900290	Genetic variants, plasma lipoprotein(a) levels, and risk of cardiovascular morbidity and mortality among two prospective cohorts of type 2 diabetes.	Lp (a) levels	1	1	1	1
rs1421085	6E-39	38.2218487496163	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs16879765	6E-39	38.2218487496163	21732829	Wnt signaling and Dupuytren's disease.	Dupuytren's disease	1	1	1	1
rs1864163	7E-39	38.1549019599857	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	HDL cholesterol	0	0	0	0
rs6056	8E-39	38.0969100130081	20031577	Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.	Fibrinogen	1	1	1	1
rs12722495	1E-38	38	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	1	1	1	1
rs1321535	1E-38	38	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs1801274	2E-38	37.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs3184504	2E-38	37.698970004336	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	1	1	1	1
rs6885099	3E-38	37.5228787452803	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs10401969	3E-38	37.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	1	1	1	1
rs900400	4E-38	37.397940008672	23202124	New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.	Birth weight	1	1	1	1
rs12946510	4E-38	37.397940008672	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs1561570	4E-38	37.397940008672	21623375	Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.	Paget's disease	1	1	1	1
rs12896399	4E-38	37.397940008672	17952075	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Blue vs. green eyes	0	1	0	0
rs8076739	5E-38	37.301029995664	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs780094	6E-38	37.2218487496164	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	1	1	1
rs2078267	9E-38	37.0457574905607	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs2076756	1E-37	37	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	0	0	1	1
rs4803750	1E-37	37	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs1260326	1E-37	37	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	1	1	1
rs10941679	2E-37	36.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs6457617	2E-37	36.698970004336	21750679	Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.	Systemic sclerosis	0	0	1	1
rs11710456	3E-37	36.5228787452803	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11741861	3E-37	36.5228787452803	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs867186	6E-37	36.2218487496164	20231535	Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium.	Coagulation factor levels	0	1	1	1
rs6120849	7E-37	36.1549019599857	20802025	Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study.	Protein C levels	0	0	0	0
rs224333	8E-37	36.096910013008	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs6065906	8E-37	36.096910013008	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs11710456	9E-37	36.0457574905607	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10995190	1E-36	36	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs217181	1E-36	36	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	1	1	1
rs3764261	1E-36	36	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	0	0	1	1
rs4077515	1E-36	36	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs3803662	1E-36	36	17529967	Genome-wide association study identifies novel breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs538656	2E-36	35.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs12896399	2E-36	35.698970004336	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Hair color	0	1	1	1
rs12511469	2E-36	35.698970004336	21757653	Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease.	Fibrinogen	0	0	0	0
rs4072037	2E-36	35.698970004336	20700443	Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.	Magnesium levels	1	1	1	1
rs1387153	2E-36	35.698970004336	19060909	A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.	Fasting plasma glucose	0	0	1	1
rs889312	3E-36	35.5228787452803	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs4713103	3E-36	35.5228787452803	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs11761528	3E-36	35.5228787452803	21533175	Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.	Dehydroepiandrosterone sulphate levels	0	1	1	1
rs9399137	3E-36	35.5228787452803	17767159	A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.	F-cell distribution	0	1	1	1
rs2155219	4E-36	35.397940008672	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs1158867	4E-36	35.397940008672	20802025	Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study.	Protein C levels	1	1	1	1
rs590856	5E-36	35.301029995664	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs2075650	5E-36	35.301029995664	20885792	Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.	Alzheimer's disease (late onset)	0	1	1	1
rs2954029	5E-36	35.301029995664	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs8050136	5E-36	35.301029995664	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	1	0	0
rs210134	7E-36	35.1549019599857	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs11742570	7E-36	35.1549019599857	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs7903146	1E-35	35	23209189	Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21.	Type 2 diabetes	0	0	1	1
rs3811647	1E-35	35	21665994	Genome-wide association study identifies two loci strongly affecting transferrin glycosylation.	Alcohol consumption (transferrin glycosylation)	0	0	0	0
rs9275572	1E-35	35	20596022	Genome-wide association study in alopecia areata implicates both innate and adaptive immunity.	Alopecia areata	0	1	1	1
rs1532085	1E-35	35	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	HDL cholesterol	0	0	1	1
rs2638315	2E-35	34.698970004336	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Metabolite levels	1	1	1	1
rs11259936	2E-35	34.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs900400	2E-35	34.698970004336	20372150	Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight.	Birth weight	0	0	1	1
rs174468	3E-35	34.5228787452803	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs3791675	3E-35	34.5228787452803	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1900004	3E-35	34.5228787452803	20548946	A genome-wide association study of optic disc parameters.	Optic disc parameters	1	1	1	1
rs1260326	3E-35	34.5228787452803	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs6426833	4E-35	34.397940008672	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	0	1	1
rs987525	5E-35	34.301029995664	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs2395029	5E-35	34.301029995664	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	0	1	1	1
rs6711012	6E-35	34.2218487496163	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs7910927	6E-35	34.2218487496163	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	0	0	0
rs1667394	6E-35	34.2218487496163	17952075	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Blond vs. brown hair color	0	1	0	0
rs10494112	7E-35	34.1549019599857	21623375	Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.	Paget's disease	1	1	1	1
rs11886868	7E-35	34.1549019599857	18245381	Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.	Fetal hemoglobin levels	1	1	1	1
rs356220	8E-35	34.0969100130081	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	0	0	1	1
rs1801133	8E-35	34.0969100130081	20031578	Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study.	Homocysteine levels	1	1	1	1
rs4794822	9E-35	34.0457574905607	21738480	Multiple loci are associated with white blood cell phenotypes.	White blood cell count	0	1	1	1
rs865686	1E-34	34	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs7258249	1E-34	34	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Sphingolipid levels	1	1	1	1
rs505922	1E-34	34	21980494	Genetics of venous thrombosis: insights from a new genome wide association study.	Venous thromboembolism	0	0	1	1
rs11107116	1E-34	34	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs16857031	1E-34	34	19305408	Common variants at ten loci influence QT interval duration in the QTGEN Study.	QT interval	0	0	0	0
rs7651446	2E-34	33.698970004336	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	1	1	1	1
rs12678919	2E-34	33.698970004336	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	HDL cholesterol	0	0	0	0
rs7903146	2E-34	33.698970004336	17293876	A genome-wide association study identifies novel risk loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs10938397	3E-34	33.5228787452803	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	1	1	1	1
rs8176704	4E-34	33.397940008672	23267103	Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.	Coagulation factor levels	0	0	0	0
rs7774434	4E-34	33.397940008672	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	0	1	1	1
rs738409	4E-34	33.397940008672	21423719	Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits.	Nonalcoholic fatty liver disease	0	1	1	1
rs10195252	4E-34	33.397940008672	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	1	1	1	1
rs4481233	6E-34	33.2218487496164	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs495366	6E-34	33.2218487496164	20031604	Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels.	Matrix metalloproteinase levels	1	1	1	1
rs7934606	7E-34	33.1549019599857	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	1	1	1	1
rs10865331	7E-34	33.1549019599857	21743469	Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.	Ankylosing spondylitis	1	1	1	1
rs8080944	8E-34	33.096910013008	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (time to first tooth eruption)	1	1	1	1
rs2413450	9E-34	33.0457574905607	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular hemoglobin	0	1	0	0
rs1015451	1E-33	33	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs7763064	1E-33	33	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs599839	1E-33	33	18262040	LDL-cholesterol concentrations: a genome-wide association study.	LDL cholesterol	0	0	1	1
rs2090409	2E-33	32.698970004336	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs798489	2E-33	32.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2187668	2E-33	32.698970004336	20694011	Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.	Immunoglobulin A 	0	1	1	1
rs1883025	2E-33	32.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs342293	2E-33	32.698970004336	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	0	0	1	1
rs6519955	3E-33	32.5228787452803	21732829	Wnt signaling and Dupuytren's disease.	Dupuytren's disease	1	1	1	1
rs9271366	3E-33	32.5228787452803	20694011	Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.	Immunoglobulin A 	0	1	1	1
rs7127900	3E-33	32.5228787452803	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	0	1	1	1
rs2413583	4E-33	32.397940008672	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs4846567	5E-33	32.301029995664	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	1	1	1	1
rs599839	6E-33	32.2218487496163	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	LDL cholesterol	0	0	1	1
rs4657178	7E-33	32.1549019599857	19305409	Common variants at ten loci modulate the QT interval duration in the QTSCD Study.	QT interval	0	0	1	1
rs16942887	8E-33	32.0969100130081	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs2395029	9E-33	32.0457574905607	19483685	HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin.	Drug-induced liver injury (flucloxacillin)	0	1	1	1
rs7554511	1E-32	32	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs9989419	1E-32	32	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs102275 	2E-32	31.698970004336	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Oleic acid (18:1n-9) plasma levels	NA	NA	NA	NA
rs1481012	2E-32	31.698970004336	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Gout	0	1	0	0
rs1800562	2E-32	31.698970004336	21665994	Genome-wide association study identifies two loci strongly affecting transferrin glycosylation.	Alcohol consumption (transferrin glycosylation)	0	1	1	1
rs9491696	2E-32	31.698970004336	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	1	1	1	1
rs3828309	2E-32	31.698970004336	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs1800588	2E-32	31.698970004336	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	HDL cholesterol	1	1	1	1
rs4246905	3E-32	31.5228787452803	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs3814113	4E-32	31.397940008672	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	1	1	1	1
rs12191877	4E-32	31.397940008672	20953188	Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2.	Psoriasis	0	0	1	1
rs1260326	4E-32	31.397940008672	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs9332998	5E-32	31.301029995664	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs11205277	5E-32	31.301029995664	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs9264942	6E-32	31.2218487496163	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	0	1	1	1
rs780094	6E-32	31.2218487496163	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs1351394	7E-32	31.1549019599857	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs1061147	7E-32	31.1549019599857	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	0	1	1
rs2235544	8E-32	31.096910013008	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs7608910	9E-32	31.0457574905607	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs7134599	9E-32	31.0457574905607	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs365132	9E-32	31.0457574905607	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs1831282	1E-31	31	23577725	Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.	Age-related macular degeneration	0	0	1	1
rs9349205	1E-31	31	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	0	1	1	1
rs995030	1E-31	31	19483681	A genome-wide association study of testicular germ cell tumor.	Testicular germ cell tumor	0	0	1	1
rs1799853	1E-31	31	19300499	A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose.	Warfarin maintenance dose	0	0	0	0
rs6065904	2E-31	30.698970004336	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	0	0	1	1
rs8078723	2E-31	30.698970004336	21738480	Multiple loci are associated with white blood cell phenotypes.	White blood cell count	0	0	0	0
rs1046934	2E-31	30.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs6511720	2E-31	30.698970004336	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	1	1	1
rs1260326	2E-31	30.698970004336	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	Triglycerides	0	0	1	1
rs7903146	2E-31	30.698970004336	17463246	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	Type 2 diabetes	0	0	1	1
rs4624820	3E-31	30.5228787452803	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	1	1	1	1
rs10936599	3E-31	30.5228787452803	23535734	Identification of seven loci affecting mean telomere length and their association with disease.	Telomere length	1	1	1	1
rs964184	3E-31	30.5228787452803	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs506585	3E-31	30.5228787452803	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs11803731	3E-31	30.5228787452803	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	0	1	1	1
rs9989419	3E-31	30.5228787452803	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	HDL cholesterol	0	0	0	0
rs11710456	4E-31	30.397940008672	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2395185	4E-31	30.397940008672	22286212	Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups.	Hodgkin's lymphoma	0	0	1	1
rs10938397	4E-31	30.397940008672	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	1	1	1
rs2981579	4E-31	30.397940008672	20453838	Genome-wide association study identifies five new breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs641153	6E-31	30.2218487496164	21665990	Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs12485738	6E-31	30.2218487496164	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	0	0	1	1
rs1427407	6E-31	30.2218487496164	17767159	A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.	F-cell distribution	0	1	1	1
rs10771399	8E-31	30.096910013008	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs7759938	8E-31	30.096910013008	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs1219648	1E-30	30	21263130	Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study.	Breast cancer	0	0	1	1
rs1250550	1E-30	30	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	1	1	1	1
rs1042034	1E-30	30	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	0	0
rs439401	1E-30	30	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	1	1
rs7903146	1E-30	30	19734900	Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia.	Type 2 diabetes and other traits	0	1	1	1
rs4973768	2E-30	29.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs174549	2E-30	29.698970004336	23281178	A genome-wide assessment of variability in human serum metabolism.	Metabolite levels	0	0	1	1
rs10922162	2E-30	29.698970004336	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	1	1	1
rs646776	2E-30	29.698970004336	21087763	Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma.	Progranulin levels	0	1	1	1
rs2731672	2E-30	29.698970004336	20303064	Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time.	Activated partial thromboplastin time	0	0	1	1
rs1800789	2E-30	29.698970004336	20031576	Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts.	Fibrinogen	0	0	1	1
rs657152	2E-30	29.698970004336	18940312	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.	Liver enzyme levels	0	1	1	1
rs1512268	3E-30	29.5228787452803	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	1	1	1	1
rs995030	3E-30	29.5228787452803	19483681	A genome-wide association study of testicular germ cell tumor.	Testicular germ cell tumor	0	0	0	0
rs4800452	4E-30	29.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs35264875	4E-30	29.397940008672	18488028	Two newly identified genetic determinants of pigmentation in Europeans.	Blond vs. brown hair color	1	1	1	1
rs12821256	4E-30	29.397940008672	17952075	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Blond vs. brown hair color	1	1	1	1
rs12116643	5E-30	29.301029995664	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	0	0	0
rs4420638	5E-30	29.301029995664	22003152	Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies.	Lipoprotein-associated phospholipase A2 activity and mass	0	0	1	1
rs12150660	6E-30	29.2218487496163	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	0	0	0
rs2657880	7E-30	29.1549019599857	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	0	1	1
rs2823286	9E-30	29.0457574905607	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs7903146	9E-30	29.0457574905607	19056611	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data.	Type 2 diabetes	0	0	1	1
rs1471633	1E-29	29	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs13300663	1E-29	29	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs10484561	1E-29	29	20639881	Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.	Follicular lymphoma	0	1	1	1
rs579459	1E-29	29	19729612	Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin.	Soluble E-selectin levels	0	1	1	1
rs7651446	2E-29	28.698970004336	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	0	0	0	0
rs10401969	2E-29	28.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	0	0
rs11153730	2E-29	28.698970004336	19587794	Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.	QT interval	1	1	1	1
rs3750848	3E-29	28.5228787452803	23577725	Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.	Age-related macular degeneration (extreme sampling)	0	1	1	1
rs6917603	3E-29	28.5228787452803	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	1	1	1	1
rs2954029	3E-29	28.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs1260326	3E-29	28.5228787452803	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs10892151	3E-29	28.5228787452803	19074352	A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection.	Triglycerides	1	1	1	1
rs646776	3E-29	28.5228787452803	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	LDL cholesterol	0	0	1	1
rs3814113	4E-29	28.397940008672	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	0	0	0	0
rs3764913	4E-29	28.397940008672	23281178	A genome-wide assessment of variability in human serum metabolism.	Metabolite levels	0	0	1	1
rs2284746	4E-29	28.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1165205	4E-29	28.397940008672	18834626	Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study.	Urate levels	0	0	1	1
rs6127471	5E-29	28.301029995664	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs2230199	5E-29	28.301029995664	21665990	Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs515135	5E-29	28.301029995664	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	LDL cholesterol	0	0	1	1
rs507666	5E-29	28.301029995664	18604267	Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women.	Soluble ICAM-1	0	0	1	1
rs11564258	6E-29	28.2218487496163	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs9832727	6E-29	28.2218487496163	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs944002	6E-29	28.2218487496163	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs1150754	6E-29	28.2218487496163	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	0	0	1	1
rs5759167	6E-29	28.2218487496163	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	1	1	1	1
rs3764261	7E-29	28.1549019599857	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	HDL cholesterol	0	0	1	1
rs2256183	8E-29	28.096910013008	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs4664308	9E-29	28.0457574905607	21323541	Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy.	Nephropathy (idiopathic membranous)	1	1	1	1
rs11225434	9E-29	28.0457574905607	20031604	Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels.	Matrix metalloproteinase levels	0	0	0	0
rs10993994	9E-29	28.0457574905607	18264097	Multiple newly identified loci associated with prostate cancer susceptibility.	Prostate cancer	1	1	1	1
rs42235	1E-28	28	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs12203592	1E-28	28	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Hair color	0	1	1	1
rs4921914	1E-28	28	21572414	A genome-wide association study of metabolic traits in human urine.	Urinary metabolites	0	1	1	1
rs2942168	1E-28	28	21292315	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.	Parkinson's disease	0	1	1	1
rs12979860	1E-28	28	19684573	Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance.	Response to hepatitis C treatment	1	1	1	1
rs10509540	1E-28	28	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs1421085	1E-28	28	19151714	Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.	Obesity	0	0	1	1
rs1171614	2E-28	27.698970004336	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs34637584	2E-28	27.698970004336	21738487	Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.	Parkinson's disease	NA	NA	NA	NA
rs12034383	2E-28	27.698970004336	21700265	Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate.	Erythrocyte sedimentation rate	1	1	1	1
rs6470764	2E-28	27.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2479409	2E-28	27.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	1	1	1	1
rs12203592	2E-28	27.698970004336	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Hair color	0	0	0	0
rs2524054	2E-28	27.698970004336	20045101	Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control.	CD4:CD8 lymphocyte ratio	0	1	1	1
rs2082412	2E-28	27.698970004336	19169254	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.	Psoriasis	1	1	1	1
rs328	2E-28	27.698970004336	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	Triglycerides	0	0	1	1
rs1421085	3E-28	27.5228787452803	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	0	1	1	1
rs1192415	3E-28	27.5228787452803	20548946	A genome-wide association study of optic disc parameters.	Optic disc parameters	1	1	1	1
rs6843082	3E-28	27.5228787452803	20173747	Common variants in KCNN3 are associated with lone atrial fibrillation.	Atrial fibrillation	0	0	1	1
rs1260326	3E-28	27.5228787452803	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs2300478	3E-28	27.5228787452803	17637780	Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.	Restless legs syndrome	0	0	1	1
rs13130484	4E-28	27.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs17810546	4E-28	27.397940008672	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	1	1	1	1
rs3807989	4E-28	27.397940008672	20062060	Genome-wide association study of PR interval.	PR interval	1	1	1	1
rs9264942	5E-28	27.301029995664	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	0	1	1	1
rs11209026	5E-28	27.301029995664	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs2187668	6E-28	27.2218487496164	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	0	1	1	1
rs3091244	6E-28	27.2218487496164	18439548	Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.	C-reactive protein	0	0	1	1
rs174448	7E-28	27.1549019599857	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs6882076	7E-28	27.1549019599857	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	1	1	1	1
rs2138852	7E-28	27.1549019599857	19110211	A genome-wide association study identifies three loci associated with mean platelet volume.	Mean platelet volume	0	0	1	1
rs2780226	8E-28	27.096910013008	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs4939827	8E-28	27.096910013008	18372901	Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.	Colorectal cancer	1	1	1	1
rs921943	9E-28	27.0457574905607	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Se levels)	1	1	1	1
rs788867	9E-28	27.0457574905607	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs12203592	9E-28	27.0457574905607	18483556	A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.	Black vs. red hair color	0	1	0	0
rs13281615	1E-27	27	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs5370	1E-27	27	23381795	Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1.	Circulating vasoactive peptide levels 	1	1	1	1
rs917727	1E-27	27	22792070	Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus.	Bone mineral density	1	1	1	1
rs236918	1E-27	27	21149283	Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.	Iron status biomarkers	1	1	1	1
rs1697421	1E-27	27	20558539	Common genetic variants associate with serum phosphorus concentration.	Phosphorus levels	0	1	1	1
rs4803750	1E-27	27	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs6763931	1E-27	27	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs10871777	2E-27	26.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs3923564	2E-27	26.698970004336	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	1	1	1	1
rs2216405	2E-27	26.698970004336	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs3129882	2E-27	26.698970004336	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	1	1	1
rs30187	2E-27	26.698970004336	21743469	Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.	Ankylosing spondylitis	1	1	1	1
rs7865618	2E-27	26.698970004336	21606135	A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.	Coronary heart disease	0	0	0	0
rs12785878	2E-27	26.698970004336	20541252	Common genetic determinants of vitamin D insufficiency: a genome-wide association study.	Vitamin D insufficiency	1	1	1	1
rs13151961	2E-27	26.698970004336	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	1	1	1	1
rs646776	2E-27	26.698970004336	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs7258249	2E-27	26.698970004336	19798445	Genetic determinants of circulating sphingolipid concentrations in European populations.	Sphingolipid levels	0	0	1	1
rs16939881	3E-27	26.5228787452803	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	1	1	1	1
rs2046045	3E-27	26.5228787452803	22494929	Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function.	Thyroid function	0	1	1	1
rs4547811	3E-27	26.5228787452803	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs258322	3E-27	26.5228787452803	21983787	Genome-wide association study identifies three new melanoma susceptibility loci.	Melanoma	0	1	1	1
rs2292239	3E-27	26.5228787452803	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	1	1	1	1
rs9470361	3E-27	26.5228787452803	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs1883025	3E-27	26.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs258322	3E-27	26.5228787452803	19578364	Genome-wide association study identifies three loci associated with melanoma risk.	Melanoma	0	0	1	1
rs3184504	3E-27	26.5228787452803	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs1172130	4E-27	26.397940008672	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs4420638	4E-27	26.397940008672	22054870	A genome-wide scan for common variants affecting the rate of age-related cognitive decline.	Cognitive decline	0	1	1	1
rs16942341	4E-27	26.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs12485738	4E-27	26.397940008672	19110211	A genome-wide association study identifies three loci associated with mean platelet volume.	Mean platelet volume	0	0	1	1
rs4420638	4E-27	26.397940008672	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	LDL cholesterol	0	0	1	1
rs6795970	5E-27	26.301029995664	23463857	Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.	Electrocardiographic conduction measures	0	1	1	1
rs8101881	6E-27	26.2218487496163	21572414	A genome-wide association study of metabolic traits in human urine.	Urinary metabolites	1	1	1	1
rs2652822	7E-27	26.1549019599857	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs1260326	7E-27	26.1549019599857	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs4613763	7E-27	26.1549019599857	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	1	1	1	1
rs10490924	8E-27	26.096910013008	23577725	Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.	Age-related macular degeneration	0	0	0	0
rs13245899	8E-27	26.096910013008	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs7460090	8E-27	26.096910013008	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs615672	8E-27	26.096910013008	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Rheumatoid arthritis	0	0	0	0
rs9989419	9E-27	26.0457574905607	20031538	Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions.	HDL cholesterol	0	0	1	1
rs3741240	1E-26	26	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	1	1	1	1
rs3091316	1E-26	26	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs8050940	1E-26	26	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs987525	1E-26	26	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	0	0	0	0
rs3184504	1E-26	26	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs6235	1E-26	26	21873549	Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.	Proinsulin levels	1	1	1	1
rs2413583	1E-26	26	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs660240	1E-26	26	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	LDL cholesterol	0	0	1	1
rs964184	1E-26	26	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs12286037	1E-26	26	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs755383	2E-26	25.698970004336	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	1	1	1	1
rs11249433	2E-26	25.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs5749482	2E-26	25.698970004336	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	NA	NA	NA	NA
rs6885099	2E-26	25.698970004336	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs7282490	2E-26	25.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs4380874	2E-26	25.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	1	1	1	1
rs1018827	2E-26	25.698970004336	21980494	Genetics of venous thrombosis: insights from a new genome wide association study.	Venous thromboembolism	0	0	1	1
rs9472155	2E-26	25.698970004336	21757650	Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels.	Vascular endothelial growth factor levels	1	1	1	1
rs6905288	2E-26	25.698970004336	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	1	1	1	1
rs2078267	2E-26	25.698970004336	20884846	Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.	Urate levels	0	0	1	1
rs1046896	2E-26	25.698970004336	20858683	Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.	Glycated hemoglobin levels	1	1	1	1
rs3782181	2E-26	25.698970004336	20543847	Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer.	Testicular germ cell cancer	0	1	1	1
rs6511720	2E-26	25.698970004336	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	LDL cholesterol	0	0	1	1
rs2395029	2E-26	25.698970004336	18369459	A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci.	Psoriasis	0	1	1	1
rs1893217	3E-26	25.5228787452803	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs6841898	3E-26	25.5228787452803	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs1378942	3E-26	25.5228787452803	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	1	1	1	1
rs8050136	3E-26	25.5228787452803	21706003	Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.	Adiposity	0	1	1	1
rs7774434	3E-26	25.5228787452803	20639880	Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis.	Primary biliary cirrhosis	0	0	1	1
rs8034191	3E-26	25.5228787452803	19654303	Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.	Lung cancer	0	1	1	1
rs11118555	4E-26	25.397940008672	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs17362588	4E-26	25.397940008672	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs4475146	4E-26	25.397940008672	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Gout	0	1	0	0
rs10105606	4E-26	25.397940008672	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs6511720	4E-26	25.397940008672	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	LDL cholesterol	0	0	1	1
rs11668344	5E-26	25.301029995664	23307926	A genome-wide association study of early menopause and the combined impact of identified variants.	Menopause (age at onset)	0	0	1	1
rs560887	5E-26	25.301029995664	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs2251746	5E-26	25.301029995664	22075330	A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study.	IgE levels 	0	1	1	1
rs10767664	5E-26	25.301029995664	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs6679677	5E-26	25.301029995664	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 1 diabetes	0	0	1	1
rs1008084	6E-26	25.2218487496163	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs1883415	6E-26	25.2218487496163	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alkaline phosphatase)	1	1	1	1
rs11708996	6E-26	25.2218487496163	20062060	Genome-wide association study of PR interval.	PR interval	1	1	1	1
rs11191548	7E-26	25.1549019599857	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	1	1	1	1
rs325	8E-26	25.0969100130081	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	HDL cholesterol	0	0	0	0
rs7014346	9E-26	25.0457574905607	18372901	Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.	Colorectal cancer	1	1	1	1
rs806794	1E-25	25	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs3793917	1E-25	25	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	0	1	1
rs506585	1E-25	25	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs6511720	1E-25	25	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs4607517	1E-25	25	19060907	Variants in MTNR1B influence fasting glucose levels.	Fasting plasma glucose	0	1	1	1
rs651007	2E-25	24.698970004336	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	0	0	0
rs3741414	2E-25	24.698970004336	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs11010067	2E-25	24.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs6638512	2E-25	24.698970004336	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	NA	NA	NA	NA
rs10758669	2E-25	24.698970004336	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs2287921	2E-25	24.698970004336	21060863	Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo.	Retinal vascular caliber	1	1	1	1
rs3135338	2E-25	24.698970004336	20159113	Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.	Multiple sclerosis	0	0	1	1
rs2292239	2E-25	24.698970004336	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs7072268	2E-25	24.698970004336	19096518	Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study.	Glycated hemoglobin levels	0	0	1	1
rs1864163	3E-25	24.5228787452803	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs855791	3E-25	24.5228787452803	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hemoglobin	0	1	0	0
rs37062	3E-25	24.5228787452803	19305408	Common variants at ten loci influence QT interval duration in the QTGEN Study.	QT interval	1	1	1	1
rs3184504	4E-25	24.397940008672	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	0	1	1	1
rs174448	4E-25	24.397940008672	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs10047462	4E-25	24.397940008672	21149283	Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.	Iron status biomarkers	0	0	0	0
rs1321313	5E-25	24.301029995664	23463857	Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.	Electrocardiographic conduction measures	0	1	1	1
rs1165196	5E-25	24.301029995664	20884846	Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.	Urate levels	0	0	1	1
rs2665838	5E-25	24.301029995664	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs6511720	5E-25	24.301029995664	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs643381	5E-25	24.301029995664	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	0	1	1	1
rs9533090	5E-25	24.301029995664	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	1	1	1	1
rs5498	5E-25	24.301029995664	18604267	Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women.	Soluble ICAM-1	0	0	0	0
rs342275	6E-25	24.2218487496164	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	0	0
rs1708299	6E-25	24.2218487496164	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs9987289	6E-25	24.2218487496164	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs41360247	6E-25	24.2218487496164	20529992	Genetic regulation of serum phytosterol levels and risk of coronary artery disease.	Phytosterol levels	1	1	1	1
rs1367117	6E-25	24.2218487496164	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs6679677	6E-25	24.2218487496164	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Rheumatoid arthritis	0	0	0	0
rs505404	7E-25	24.1549019599857	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs662138	7E-25	24.1549019599857	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs3129900	7E-25	24.1549019599857	20639878	A genome-wide study identifies HLA alleles associated with lumiracoxib-related liver injury.	Lumiracoxib-related liver injury	0	1	1	1
rs7188697	7E-25	24.1549019599857	19305409	Common variants at ten loci modulate the QT interval duration in the QTSCD Study.	QT interval	0	0	1	1
rs887829	9E-25	24.0457574905607	23281178	A genome-wide assessment of variability in human serum metabolism.	Metabolite levels	0	1	1	1
rs643434	9E-25	24.0457574905607	22291609	A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.	Inflammatory biomarkers	0	1	1	1
rs1458038	9E-25	24.0457574905607	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	1	1	1	1
rs984222	9E-25	24.0457574905607	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	1	1	1	1
rs9967417	9E-25	24.0457574905607	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs753760	1E-24	24	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs909674	1E-24	24	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1641537	1E-24	24	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	1	1	1	1
rs1972809	1E-24	24	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	NA	NA	NA	NA
rs10914144	1E-24	24	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs1055144	1E-24	24	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	1	1	1	1
rs342293	1E-24	24	19221038	A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function.	Mean platelet volume	0	0	1	1
rs210138	2E-24	23.698970004336	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	0	1	1	1
rs3118906	2E-24	23.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs10761731	2E-24	23.698970004336	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	0	0
rs2145272	2E-24	23.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2079795	2E-24	23.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs4242384	2E-24	23.698970004336	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	1	1	1	1
rs11970286	2E-24	23.698970004336	19305409	Common variants at ten loci modulate the QT interval duration in the QTSCD Study.	QT interval	0	0	1	1
rs6564851	2E-24	23.698970004336	19185284	Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study.	Carotenoid and tocopherol levels	1	1	1	1
rs11855019	2E-24	23.698970004336	18483556	A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.	Black vs. blond hair color	NA	NA	NA	NA
rs6440003	2E-24	23.698970004336	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs2227631	3E-24	23.5228787452803	22990020	Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation.	Plasminogen activator inhibitor type 1 levels (PAI-1)	1	1	1	1
rs9552416	3E-24	23.5228787452803	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	1	1	1	1
rs1333049	3E-24	23.5228787452803	22144573	Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.	Coronary artery calcification	0	1	1	1
rs2242652	3E-24	23.5228787452803	21743467	Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.	Prostate cancer	1	1	1	1
rs2000999	3E-24	23.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	1	1
rs780094	3E-24	23.5228787452803	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	0	0	0
rs780094	3E-24	23.5228787452803	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting insulin-related traits	0	1	0	0
rs987525	3E-24	23.5228787452803	19270707	Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.	Orofacial clefts	0	0	1	1
rs2066847	3E-24	23.5228787452803	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	NA	NA	NA	NA
rs3796619	3E-24	23.5228787452803	18239089	Sequence variants in the RNF212 gene associate with genome-wide recombination rate.	Recombination rate (males)	1	1	1	1
rs3793917	4E-24	23.397940008672	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	0	0	0
rs780094	4E-24	23.397940008672	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs2479409	4E-24	23.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs8396	4E-24	23.397940008672	20037589	A genome-wide perspective of genetic variation in human metabolism.	Metabolite levels	1	1	1	1
rs1260326	4E-24	23.397940008672	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs4635969	5E-24	23.301029995664	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	1	1	1	1
rs1532085	5E-24	23.301029995664	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs174546	5E-24	23.301029995664	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	1	1
rs964184	5E-24	23.301029995664	20657596	Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.	Hypertriglyceridemia	0	1	1	1
rs484959	5E-24	23.301029995664	20436471	Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.	Paget's disease	0	0	1	1
rs7980799	6E-24	23.2218487496163	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs10189761	6E-24	23.2218487496163	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs6885099	6E-24	23.2218487496163	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs2731672	6E-24	23.2218487496163	23381795	Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1.	Circulating vasoactive peptide levels 	0	0	0	0
rs4420638	6E-24	23.2218487496163	20442857	Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study.	Lipoprotein-associated phospholipase A2 activity and mass	0	0	1	1
rs4481887	7E-24	23.1549019599857	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs11191548	7E-24	23.1549019599857	19430483	Genome-wide association study identifies eight loci associated with blood pressure.	Systolic blood pressure	0	0	1	1
rs6679677	8E-24	23.096910013008	17554260	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.	Type 1 diabetes	0	0	0	0
rs1831282	9E-24	23.0457574905607	23577725	Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.	Age-related macular degeneration (extreme sampling)	0	1	0	0
rs2108622	9E-24	23.0457574905607	23281178	A genome-wide assessment of variability in human serum metabolism.	Metabolite levels	1	1	1	1
rs909674	9E-24	23.0457574905607	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs9987289	9E-24	23.0457574905607	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs2228671	9E-24	23.0457574905607	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	0	1	1
rs57024841	1E-23	23	23328707	Genome-wide significant locus of beta-trace protein, a novel kidney function biomarker, identified in European and African Americans.	Beta-trace protein levels	1	1	1	1
rs675209	1E-23	23	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs6062504	1E-23	23	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs17346452	1E-23	23	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs3812163	1E-23	23	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs247616	1E-23	23	20838585	Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.	Cardiovascular disease risk factors	0	0	1	1
rs4635969	1E-23	23	20543847	Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer.	Testicular germ cell cancer	0	1	1	1
rs755383	1E-23	23	20543847	Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer.	Testicular germ cell cancer	0	1	1	1
rs1800562	1E-23	23	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Hematological parameters	0	1	1	1
rs1378942	1E-23	23	19430483	Genome-wide association study identifies eight loci associated with blood pressure.	Diastolic blood pressure	0	0	1	1
rs9264638	2E-23	22.698970004336	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	0	1	1	1
rs1302019	2E-23	22.698970004336	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs6742078	2E-23	22.698970004336	22511988	A genome-wide association study identifies UGT1A1 as a regulator of serum cell-free DNA in young adults: The Cardiovascular Risk in Young Finns Study.	Circulating cell-free DNA	0	1	1	1
rs1805017	2E-23	22.698970004336	22003152	Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies.	Lipoprotein-associated phospholipase A2 activity and mass	1	1	1	1
rs1458038	2E-23	22.698970004336	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	0	1	0	0
rs9332739	2E-23	22.698970004336	21665990	Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.	Age-related macular degeneration	0	0	0	0
rs12896399	2E-23	22.698970004336	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Eye color	0	1	1	1
rs10516526	2E-23	22.698970004336	20010834	Genome-wide association study identifies five loci associated with lung function.	Pulmonary function	1	1	1	1
rs258322	2E-23	22.698970004336	18483556	A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.	Black vs. red hair color	0	1	1	1
rs9888739	2E-23	22.698970004336	18204446	Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.	Systemic lupus erythematosus	1	1	1	1
rs12203592	3E-23	22.5228787452803	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Tanning	0	1	0	0
rs1004446	3E-23	22.5228787452803	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	0	0	0
rs1449263	3E-23	22.5228787452803	21738480	Multiple loci are associated with white blood cell phenotypes.	White blood cell count	1	1	1	1
rs7903146	3E-23	22.5228787452803	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs9940128	4E-23	22.397940008672	23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Body mass index	0	0	1	1
rs11205303	4E-23	22.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs798554	4E-23	22.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs6015450	4E-23	22.397940008672	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	1	1	1	1
rs543874	4E-23	22.397940008672	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs3093030	4E-23	22.397940008672	20167578	Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels.	Soluble levels of adhesion molecules	0	1	1	1
rs9268877	4E-23	22.397940008672	19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Ulcerative colitis	0	0	1	1
rs560887	4E-23	22.397940008672	18451265	A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels.	Fasting plasma glucose	0	0	1	1
rs140522	5E-23	22.301029995664	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs6993770	5E-23	22.301029995664	21757650	Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels.	Vascular endothelial growth factor levels	1	1	1	1
rs11248850	6E-23	22.2218487496164	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs4500751	6E-23	22.2218487496164	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs7923609	6E-23	22.2218487496164	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alkaline phosphatase)	0	1	1	1
rs6015450	6E-23	22.2218487496164	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	0	1	0	0
rs1378942	6E-23	22.2218487496164	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	0	1	0	0
rs9428104	6E-23	22.2218487496164	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2361502	7E-23	22.1549019599857	21646302	Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels.	Bilirubin levels	0	0	0	0
rs646776	8E-23	22.0969100130081	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	LDL cholesterol	0	0	1	1
rs10468017	8E-23	22.0969100130081	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	HDL cholesterol	0	0	1	1
rs2282978	8E-23	22.0969100130081	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs633715	9E-23	22.0457574905607	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs12621278	9E-23	22.0457574905607	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	1	1	1	1
rs693	9E-23	22.0457574905607	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	0	1	1
rs328	9E-23	22.0457574905607	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	HDL cholesterol	0	0	0	0
rs174549	1E-22	22	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	0	1	1	1
rs12913832	1E-22	22	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Tanning	0	1	0	0
rs11847263	1E-22	22	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs12593813	1E-22	22	21779176	Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.	Restless legs syndrome	1	1	1	1
rs4977574	1E-22	22	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	0	1	1
rs1552224	1E-22	22	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	0	1	1	1
rs9390459	1E-22	22	20231535	Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium.	Coagulation factor levels	1	1	1	1
rs2138852	1E-22	22	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	0	0	1	1
rs17356907	2E-22	21.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs9260489	2E-22	21.698970004336	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	NA	NA	NA	NA
rs10445033	2E-22	21.698970004336	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs12740374	2E-22	21.698970004336	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity and mass	0	1	1	1
rs6025	2E-22	21.698970004336	22672568	A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.	Venous thromboembolism	0	0	1	1
rs6258	2E-22	21.698970004336	21998597	Genetic determinants of serum testosterone concentrations in men.	Testosterone levels	0	1	1	1
rs660240	2E-22	21.698970004336	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	1	1	1
rs2023634	2E-22	21.698970004336	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs10980800	2E-22	21.698970004336	21738480	Multiple loci are associated with white blood cell phenotypes.	White blood cell count	1	1	1	1
rs2836878	2E-22	21.698970004336	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs2815752	2E-22	21.698970004336	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs17251221	2E-22	21.698970004336	20705733	Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.	Calcium levels	1	1	1	1
rs174546	2E-22	21.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs174546	2E-22	21.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	0	0
rs6065906	2E-22	21.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	1	1
rs2000999	2E-22	21.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs6882076	2E-22	21.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs10440833	2E-22	21.698970004336	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	1	1	1	1
rs1333040	2E-22	21.698970004336	20364137	Genome-wide association study of intracranial aneurysm identifies three new risk loci.	Intracranial aneurysm	0	1	1	1
rs506585	2E-22	21.698970004336	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs11796357	3E-22	21.5228787452803	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (time to first tooth eruption)	NA	NA	NA	NA
rs6845078	3E-22	21.5228787452803	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs2030323	3E-22	21.5228787452803	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs11152213	3E-22	21.5228787452803	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs9272143	3E-22	21.5228787452803	23482656	Genome-wide association study of susceptibility loci for cervical cancer.	Cervical cancer	NA	NA	NA	NA
rs1536482	3E-22	21.5228787452803	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs2051549	3E-22	21.5228787452803	23053960	Genome-wide pathway analysis of genome-wide association studies on systemic lupus erythematosus and rheumatoid arthritis.	Systemic lupus erythematosus	0	1	1	1
rs2160387	3E-22	21.5228787452803	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Metabolite levels	1	1	1	1
rs2497938	3E-22	21.5228787452803	22032556	Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness.	Male-pattern baldness	NA	NA	NA	NA
rs4149081	3E-22	21.5228787452803	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs1154155	3E-22	21.5228787452803	19412176	Narcolepsy is strongly associated with the T-cell receptor alpha locus.	Narcolepsy	1	1	1	1
rs2794520	3E-22	21.5228787452803	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	Metabolic traits	0	1	1	1
rs9349379	4E-22	21.397940008672	22144573	Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.	Coronary artery calcification	1	1	1	1
rs10761659	4E-22	21.397940008672	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs2896526	4E-22	21.397940008672	21124955	Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A.	Amyloid A Levels	1	1	1	1
rs8079702	4E-22	21.397940008672	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (time to first tooth eruption)	0	0	1	1
rs10503669	4E-22	21.397940008672	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs2206277	5E-22	21.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	1	1	1	1
rs261334	5E-22	21.301029995664	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs2453533	5E-22	21.301029995664	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs10494366	5E-22	21.301029995664	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	1	1	1
rs11756438	5E-22	21.301029995664	19305408	Common variants at ten loci influence QT interval duration in the QTGEN Study.	QT interval	0	0	1	1
rs9286879	6E-22	21.2218487496164	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs12942547	6E-22	21.2218487496164	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs713586	6E-22	21.2218487496164	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs2580816	6E-22	21.2218487496164	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs7274811	6E-22	21.2218487496164	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs12447690	6E-22	21.2218487496164	20719862	New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.	Central corneal thickness	0	1	1	1
rs4785763	6E-22	21.2218487496164	19578364	Genome-wide association study identifies three loci associated with melanoma risk.	Melanoma	0	1	1	1
rs562338	6E-22	21.2218487496164	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	LDL cholesterol	0	0	1	1
rs704010	7E-22	21.1549019599857	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs10936632	7E-22	21.1549019599857	21743467	Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.	Prostate cancer	1	1	1	1
rs10401969	7E-22	21.1549019599857	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs11708067	7E-22	21.1549019599857	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	1	1	1	1
rs1864163	7E-22	21.1549019599857	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs17145738	7E-22	21.1549019599857	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	Triglycerides	0	0	1	1
rs2024092	8E-22	21.096910013008	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs9357271	8E-22	21.096910013008	21779176	Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.	Restless legs syndrome	1	1	1	1
rs635634	8E-22	21.096910013008	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	1	1
rs724016	8E-22	21.096910013008	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	0	0	1	1
rs1292011	9E-22	21.0457574905607	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs4654925	9E-22	21.0457574905607	20228798	Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL).	Ulcerative colitis	0	0	1	1
rs646776	9E-22	21.0457574905607	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	0	0	0
rs2070600	1E-21	21	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	1	1	1	1
rs6920220	1E-21	21	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs26528	1E-21	21	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs6871626	1E-21	21	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs6569648	1E-21	21	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs174546	1E-21	21	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs6904029	1E-21	21	20410501	Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.	Vitiligo	1	1	1	1
rs710446	1E-21	21	20303064	Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time.	Activated partial thromboplastin time	0	0	1	1
rs16991615	1E-21	21	19448621	Genome-wide association studies identify loci associated with age at menarche and age at natural menopause.	Menarche and menopause (age at onset)	0	1	1	1
rs16998073	1E-21	21	19430483	Genome-wide association study identifies eight loci associated with blood pressure.	Diastolic blood pressure	0	0	1	1
rs4910742	1E-21	21	18245381	Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.	Fetal hemoglobin levels	1	1	1	1
rs693	1E-21	21	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	LDL cholesterol	0	0	1	1
rs2076756	1E-21	21	17684544	Systematic association mapping identifies NELL1 as a novel IBD disease gene.	Crohn's disease	0	0	1	1
rs3757318	2E-21	20.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs3764147	2E-21	20.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs1625895	2E-21	20.698970004336	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	1	1	1	1
rs1558324	2E-21	20.698970004336	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs2647012	2E-21	20.698970004336	21533074	GWAS of follicular lymphoma reveals allelic heterogeneity at 6p21.32 and suggests shared genetic susceptibility with diffuse large B-cell lymphoma.	Follicular lymphoma	0	0	1	1
rs3764419	2E-21	20.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1173727	2E-21	20.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs6426833	2E-21	20.698970004336	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	0	0	1	1
rs13376333	2E-21	20.698970004336	20173747	Common variants in KCNN3 are associated with lone atrial fibrillation.	Atrial fibrillation	1	1	1	1
rs2476601	2E-21	20.698970004336	19503088	REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.	Rheumatoid arthritis	0	0	1	1
rs1799990	2E-21	20.698970004336	19081515	Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.	Creutzfeldt-Jakob disease	1	1	1	1
rs9594759	2E-21	20.698970004336	18445777	Multiple genetic loci for bone mineral density and fractures.	Bone mineral density (spine)	0	0	1	1
rs11847263	3E-21	20.5228787452803	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs3749171	3E-21	20.5228787452803	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs6857559	3E-21	20.5228787452803	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs2191349	3E-21	20.5228787452803	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs2925979	3E-21	20.5228787452803	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	1	1	1	1
rs34778348	3E-21	20.5228787452803	22438815	Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.	Parkinson's disease	NA	NA	NA	NA
rs1934179	3E-21	20.5228787452803	21113153	Common variants in DGKK are strongly associated with risk of hypospadias.	Hypospadias	NA	NA	NA	NA
rs12444979	3E-21	20.5228787452803	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs2871865	3E-21	20.5228787452803	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs429608	3E-21	20.5228787452803	20385819	Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs2393967	3E-21	20.5228787452803	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	0	0	1	1
rs2187668	3E-21	20.5228787452803	18204098	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.	Systemic lupus erythematosus	0	0	1	1
rs3825942	3E-21	20.5228787452803	17690259	Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma.	Glaucoma (exfoliation)	1	1	1	1
rs8089364	4E-21	20.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Body mass index	0	0	0	0
rs7689420	4E-21	20.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs10799824	4E-21	20.397940008672	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs12899618	4E-21	20.397940008672	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	1	1	1	1
rs1656966	4E-21	20.397940008672	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	0	1	1	1
rs7903146	4E-21	20.397940008672	22693455	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.	Type 2 diabetes	0	0	0	0
rs11209026	4E-21	20.397940008672	22293688	1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.	Crohn's disease	0	0	1	1
rs700752	4E-21	20.397940008672	21216879	A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3.	Insulin-like growth factors	1	1	1	1
rs1490384	4E-21	20.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs4938303	4E-21	20.397940008672	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs4846914	4E-21	20.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs4420638	4E-21	20.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	0	0
rs4796217	4E-21	20.397940008672	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs1126809	5E-21	20.301029995664	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Tanning	NA	NA	NA	NA
rs4295627	5E-21	20.301029995664	21531791	Chromosome 7p11.2 (EGFR) variation influences glioma risk.	Glioma	1	1	1	1
rs11564258	6E-21	20.2218487496163	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs2524054	6E-21	20.2218487496163	20045101	Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control.	CD4:CD8 lymphocyte ratio	0	0	0	0
rs3764261	7E-21	20.1549019599857	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity and mass	0	1	1	1
rs1819333	7E-21	20.1549019599857	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs653178	7E-21	20.1549019599857	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs1892534	7E-21	20.1549019599857	18439548	Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.	C-reactive protein	0	0	1	1
rs11153730	8E-21	20.096910013008	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	0	1	1	1
rs4900109	8E-21	20.096910013008	21835309	GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development.	Iris characteristics	0	1	1	1
rs3018362	8E-21	20.096910013008	21623375	Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.	Paget's disease	1	1	1	1
rs6584283	8E-21	20.096910013008	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs4962153	8E-21	20.096910013008	18940312	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.	Liver enzyme levels	0	1	1	1
rs12896399	8E-21	20.096910013008	18483556	A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.	Black vs. blond hair color	0	1	1	1
rs443198	9E-21	20.0457574905607	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	1	1	1
rs635634	9E-21	20.0457574905607	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs769449	9E-21	20.0457574905607	18439548	Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.	C-reactive protein	0	0	1	1
rs7741741	1E-20	20	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs7138803	1E-20	20	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	1	1	1	1
rs102275	1E-20	20	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Stearic acid (18:0) plasma levels	0	1	1	1
rs9939609	1E-20	20	22693455	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.	Type 2 diabetes	0	1	1	1
rs9430161	1E-20	20	22327514	Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma.	Ewing sarcoma	1	1	1	1
rs2403254	1E-20	20	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs1229984	1E-20	20	21437268	A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium.	Upper aerodigestive tract cancers	1	1	1	1
rs6017342	1E-20	20	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	0	1	1
rs12521868	1E-20	20	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs2546890	1E-20	20	20953188	Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2.	Psoriasis	0	0	1	1
rs33980500	1E-20	20	20953186	Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis.	Psoriatic arthritis	1	1	1	1
rs237743	1E-20	20	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1799884	1E-20	20	20858683	Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.	Glycated hemoglobin levels	0	1	1	1
rs2040406	1E-20	20	20453840	Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs12917707	1E-20	20	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs7499892	1E-20	20	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs1059611	1E-20	20	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	1	1	1
rs1668873	1E-20	20	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	0	0	1	1
rs17728338	1E-20	20	19169254	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.	Psoriasis	1	1	1	1
rs4420638	1E-20	20	18262040	LDL-cholesterol concentrations: a genome-wide association study.	LDL cholesterol	0	0	1	1
rs12654264	1E-20	20	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	LDL cholesterol	0	0	1	1
rs10757278	1E-20	20	17478679	A common variant on chromosome 9p21 affects the risk of myocardial infarction.	Myocardial infarction	0	1	1	1
rs9271640	2E-20	19.698970004336	23472185	Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.	Multiple sclerosis (OCB status)	0	1	1	1
rs4420638	2E-20	19.698970004336	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	0	1	1	1
rs7652995	2E-20	19.698970004336	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2075672	2E-20	19.698970004336	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs1667394	2E-20	19.698970004336	23118974	Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations.	Eye color	0	0	1	1
rs1341665	2E-20	19.698970004336	22291609	A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.	Inflammatory biomarkers	0	1	1	1
rs7903146	2E-20	19.698970004336	21873549	Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.	Proinsulin levels	0	1	1	1
rs987870	2E-20	19.698970004336	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	1	1	1
rs7574865	2E-20	19.698970004336	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	1	1	1	1
rs1801274	2E-20	19.698970004336	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs4409764	2E-20	19.698970004336	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs7359397	2E-20	19.698970004336	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	1	1	1
rs10748128	2E-20	19.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs515135	2E-20	19.698970004336	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	LDL cholesterol	0	0	1	1
rs641153	2E-20	19.698970004336	20385826	Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).	Age-related macular degeneration	0	0	1	1
rs646776	2E-20	19.698970004336	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs6544713	2E-20	19.698970004336	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	LDL cholesterol	0	0	1	1
rs872071	2E-20	19.698970004336	18758461	A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia.	Chronic lymphocytic leukemia	1	1	1	1
rs2251746	2E-20	19.698970004336	18846228	Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus.	IgE levels 	0	0	1	1
rs4704397	2E-20	19.698970004336	18514160	Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function.	Thyroid stimulating hormone	0	1	1	1
rs2292239	2E-20	19.698970004336	17554260	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.	Type 1 diabetes	0	0	1	1
rs9939609	2E-20	19.698970004336	17434869	A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity.	Body mass index	0	0	1	1
rs2769264	3E-20	19.5228787452803	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Cu levels)	1	1	1	1
rs17287293	3E-20	19.5228787452803	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs1805126	3E-20	19.5228787452803	23463857	Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.	Electrocardiographic conduction measures	0	1	1	1
rs917997	3E-20	19.5228787452803	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs11558471	3E-20	19.5228787452803	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	1	1	1	1
rs10799701	3E-20	19.5228787452803	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs10098310	3E-20	19.5228787452803	21738480	Multiple loci are associated with white blood cell phenotypes.	White blood cell count	0	1	1	1
rs987237	3E-20	19.5228787452803	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	1	1	1
rs1800562	3E-20	19.5228787452803	20858683	Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.	Glycated hemoglobin levels	0	1	1	1
rs10741657	3E-20	19.5228787452803	20541252	Common genetic determinants of vitamin D insufficiency: a genome-wide association study.	Vitamin D insufficiency	1	1	1	1
rs1532624	3E-20	19.5228787452803	20066028	Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels.	Cholesterol	0	1	1	1
rs1980057	3E-20	19.5228787452803	20010835	Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.	Pulmonary function	1	1	1	1
rs10758658	3E-20	19.5228787452803	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	0	1	1	1
rs602662	3E-20	19.5228787452803	19303062	Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations.	Folate pathway vitamin levels	0	1	1	1
rs780094	3E-20	19.5228787452803	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Triglycerides	0	0	1	1
rs1042725	3E-20	19.5228787452803	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	0	0	1	1
rs4775041	3E-20	19.5228787452803	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs4489968	4E-20	19.397940008672	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs10159477	4E-20	19.397940008672	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs7607980	4E-20	19.397940008672	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	0	1	1	1
rs503279	4E-20	19.397940008672	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs4502156	4E-20	19.397940008672	21873549	Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.	Proinsulin levels	1	1	1	1
rs16891982	4E-20	19.397940008672	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Hair color	1	1	1	1
rs780094	4E-20	19.397940008672	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	0	0	0
rs780094	4E-20	19.397940008672	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting insulin-related traits	0	0	0	0
rs10995271	4E-20	19.397940008672	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs7090512	5E-20	19.301029995664	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs12429889	5E-20	19.301029995664	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs240993	5E-20	19.301029995664	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	1	1	1	1
rs7578326	5E-20	19.301029995664	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	1	1	1	1
rs8034191	5E-20	19.301029995664	18385738	A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25.	Lung cancer	0	0	1	1
rs753760	6E-20	19.2218487496164	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs1354774	6E-20	19.2218487496164	23359319	Genome-wide association study identifies loci at ATF7IP and KLK2 associated with percentage of circulating free PSA.	Prostate-specific antigen levels	1	1	1	1
rs9883204	6E-20	19.2218487496164	23202124	New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.	Birth weight	0	1	1	1
rs10262453	6E-20	19.2218487496164	23160099	A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.	Sagittal craniosynostosis	1	1	1	1
rs780094	6E-20	19.2218487496164	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs7692808	6E-20	19.2218487496164	20062060	Genome-wide association study of PR interval.	PR interval	1	1	1	1
rs11855019	6E-20	19.2218487496164	18483556	A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.	Black vs. red hair color	NA	NA	NA	NA
rs1051730	6E-20	19.2218487496164	18385739	A variant associated with nicotine dependence, lung cancer and peripheral arterial disease.	Nicotine dependence	0	1	1	1
rs633715	7E-20	19.1549019599857	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs339969	7E-20	19.1549019599857	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs653178	7E-20	19.1549019599857	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs889312	7E-20	19.1549019599857	17529967	Genome-wide association study identifies novel breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs11847263	8E-20	19.0969100130081	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs741702	8E-20	19.0969100130081	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs6568421	8E-20	19.0969100130081	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs921720	8E-20	19.0969100130081	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs964184	8E-20	19.0969100130081	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	1	1	1
rs651821	8E-20	19.0969100130081	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	0	1	1	1
rs4329	8E-20	19.0969100130081	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs2242944	8E-20	19.0969100130081	20062062	Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.	Ankylosing spondylitis	0	1	1	1
rs9349205	8E-20	19.0969100130081	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular hemoglobin	0	1	0	0
rs887829	9E-20	19.0457574905607	23642732	Association of SNPs in the UGT1A gene cluster with total bilirubin and mortality in the Diabetes Heart Study.	Bilirubin levels	0	0	1	1
rs1532085	9E-20	19.0457574905607	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs2076295	1E-19	19	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	1	1	1	1
rs11259933	1E-19	19	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs2236496	1E-19	19	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs1042725	1E-19	19	23202124	New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.	Birth weight	0	1	1	1
rs72669744	1E-19	19	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	1	1	1	1
rs17319721	1E-19	19	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs1532085	1E-19	19	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	1	1
rs3123078	1E-19	19	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	0	0	1	1
rs4132601	1E-19	19	19684604	Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs2187668	1E-19	19	17558408	A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.	Celiac disease	0	0	1	1
rs8080944	2E-19	18.698970004336	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (number of teeth)	0	1	0	0
rs2736100	2E-19	18.698970004336	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	0	1	1	1
rs1805007	2E-19	18.698970004336	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Sunburns	0	1	0	0
rs11847263	2E-19	18.698970004336	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs925489	2E-19	18.698970004336	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	1	1	1	1
rs13106975	2E-19	18.698970004336	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Sphingolipid levels	1	1	1	1
rs4693089	2E-19	18.698970004336	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs2277339	2E-19	18.698970004336	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs13129697	2E-19	18.698970004336	22229870	Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia.	Uric acid levels	0	0	1	1
rs356220	2E-19	18.698970004336	21738487	Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.	Parkinson's disease	0	0	1	1
rs4410790	2E-19	18.698970004336	21490707	Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.	Caffeine consumption	1	1	1	1
rs10931468	2E-19	18.698970004336	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	1	1	1	1
rs1260333	2E-19	18.698970004336	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs7241918	2E-19	18.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs10865331	2E-19	18.698970004336	20062062	Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.	Ankylosing spondylitis	0	0	1	1
rs1447295	2E-19	18.698970004336	19767754	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.	Prostate cancer	0	0	1	1
rs1172822	2E-19	18.698970004336	19448621	Genome-wide association studies identify loci associated with age at menarche and age at natural menopause.	Menarche and menopause (age at onset)	0	1	1	1
rs157580	2E-19	18.698970004336	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	LDL cholesterol	0	1	1	1
rs2207139	3E-19	18.5228787452803	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs999737	3E-19	18.5228787452803	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs3211770	3E-19	18.5228787452803	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	0	0	0
rs7410943	3E-19	18.5228787452803	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	0	0	0
rs4953318	3E-19	18.5228787452803	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs9389269	3E-19	18.5228787452803	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs1362931	3E-19	18.5228787452803	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity and mass	0	0	1	1
rs17085007	3E-19	18.5228787452803	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs1497406	3E-19	18.5228787452803	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs17279437	3E-19	18.5228787452803	21572414	A genome-wide association study of metabolic traits in human urine.	Urinary metabolites	1	1	1	1
rs2637125	3E-19	18.5228787452803	21533175	Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.	Dehydroepiandrosterone sulphate levels	1	1	1	1
rs653178	3E-19	18.5228787452803	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	0	1	1	1
rs10781499	3E-19	18.5228787452803	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs17293632	3E-19	18.5228787452803	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	1	1	1	1
rs6029526	3E-19	18.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	1	1	1	1
rs2395029	3E-19	18.5228787452803	19115949	Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02).	AIDS progression	0	1	1	1
rs3846662	3E-19	18.5228787452803	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	0	1	1
rs2075650	3E-19	18.5228787452803	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	0	1	1
rs2954029	3E-19	18.5228787452803	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	Triglycerides	0	0	1	1
rs4242382	3E-19	18.5228787452803	18264096	Multiple loci identified in a genome-wide association study of prostate cancer.	Prostate cancer	0	0	1	1
rs1333049	3E-19	18.5228787452803	17634449	Genomewide association analysis of coronary artery disease.	Coronary heart disease	0	0	1	1
rs633715	4E-19	18.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs3184504	4E-19	18.397940008672	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs1260326	4E-19	18.397940008672	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	0	1	1	1
rs17114036	4E-19	18.397940008672	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	1	1	1	1
rs3177928	4E-19	18.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	1	1
rs9479482	4E-19	18.397940008672	20596022	Genome-wide association study in alopecia areata implicates both innate and adaptive immunity.	Alopecia areata	1	1	1	1
rs2327832	4E-19	18.397940008672	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs12537284	4E-19	18.397940008672	18204446	Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.	Systemic lupus erythematosus	1	1	1	1
rs10503669	4E-19	18.397940008672	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	HDL cholesterol	0	0	0	0
rs7652995	5E-19	18.301029995664	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2521501	5E-19	18.301029995664	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	1	1	1	1
rs12566888	5E-19	18.301029995664	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	1	1	1	1
rs3814113	5E-19	18.301029995664	19648919	A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.	Ovarian cancer	0	0	1	1
rs1558902	5E-19	18.301029995664	19557197	NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium.	Waist circumference	0	1	1	1
rs930847	6E-19	18.2218487496163	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs11264341	6E-19	18.2218487496163	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs16940202	6E-19	18.2218487496163	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	1	1	1	1
rs2954029	6E-19	18.2218487496163	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	0	0
rs1800562	6E-19	18.2218487496163	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hemoglobin	0	1	0	0
rs3803662	6E-19	18.2218487496163	17529974	Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer.	Breast cancer	0	0	1	1
rs11796357	7E-19	18.1549019599857	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (number of teeth)	NA	NA	NA	NA
rs12821256	7E-19	18.1549019599857	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Hair color	0	1	1	1
rs4915559	7E-19	18.1549019599857	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	0	0	0
rs11717368	7E-19	18.1549019599857	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs3806156	7E-19	18.1549019599857	20410501	Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.	Vitiligo	0	1	1	1
rs11970772	7E-19	18.1549019599857	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Hematological parameters	0	1	1	1
rs7089424	7E-19	18.1549019599857	19684604	Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs3184504	7E-19	18.1549019599857	19198610	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.	Eosinophil counts	0	1	1	1
rs7714584	8E-19	18.096910013008	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs10938494	8E-19	18.096910013008	19798445	Genetic determinants of circulating sphingolipid concentrations in European populations.	Sphingolipid levels	0	0	1	1
rs6001930	9E-19	18.0457574905607	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs3104767	9E-19	18.0457574905607	21779176	Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.	Restless legs syndrome	0	1	1	1
rs445925	9E-19	18.0457574905607	20838585	Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.	Cardiovascular disease risk factors	0	1	1	1
rs266717	9E-19	18.0457574905607	20011104	A genome-wide association study reveals variants in ARL15 that influence adiponectin levels.	Adiponectin levels	0	0	1	1
rs10004195	1E-18	18	23652523	Identification of genetic loci associated with Helicobacter pylori serologic status.	Helicobacter pylori serologic status	1	1	1	1
rs2079795	1E-18	18	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs11209026	1E-18	18	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	0	0	1	1
rs6499165	1E-18	18	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs11153730	1E-18	18	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	0	1	1	1
rs2241423	1E-18	18	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	1	1	1
rs613872	1E-18	18	20825314	E2-2 protein and Fuchs's corneal dystrophy.	Fuchs's corneal dystrophy	1	1	1	1
rs6548238	1E-18	18	19079261	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.	Body mass index	0	0	1	1
rs2120019	2E-18	17.698970004336	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Zn levels)	1	1	1	1
rs769449	2E-18	17.698970004336	23562540	GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.	Alzheimer's disease biomarkers	0	1	1	1
rs6675668	2E-18	17.698970004336	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Stearic acid (18:0) plasma levels	1	1	1	1
rs6931514	2E-18	17.698970004336	23202124	New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.	Birth weight	0	1	1	1
rs11879191	2E-18	17.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs7428796	2E-18	17.698970004336	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs4561508	2E-18	17.698970004336	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum total protein level	1	1	1	1
rs1593	2E-18	17.698970004336	22703881	Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.	Activated partial thromboplastin time	0	1	1	1
rs4078978	2E-18	17.698970004336	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs2157719	2E-18	17.698970004336	22570617	Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.	Glaucoma (primary open-angle)	0	1	1	1
rs1169288	2E-18	17.698970004336	22010049	Loci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations.	Gamma gluatamyl transferase levels	0	1	1	1
rs4590817	2E-18	17.698970004336	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	1	1	1	1
rs9642880	2E-18	17.698970004336	20972438	A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.	Bladder cancer	1	1	1	1
rs9816226	2E-18	17.698970004336	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs17511102	2E-18	17.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs10037512	2E-18	17.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1950500	2E-18	17.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1393350	2E-18	17.698970004336	20410501	Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.	Vitiligo	1	1	1	1
rs7944584	2E-18	17.698970004336	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	1	1	1
rs11226373	2E-18	17.698970004336	20031604	Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels.	Matrix metalloproteinase levels	1	1	1	1
rs4295627	2E-18	17.698970004336	19578367	Genome-wide association study identifies five susceptibility loci for glioma.	Glioma	0	0	1	1
rs2231142	2E-18	17.698970004336	19503597	Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.	Uric acid levels	0	1	1	1
rs7561317	2E-18	17.698970004336	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	1	1	1
rs10096633	2E-18	17.698970004336	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Triglycerides	0	0	1	1
rs2188962	2E-18	17.698970004336	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs4896582	2E-18	17.698970004336	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	0	0	1	1
rs2735839	2E-18	17.698970004336	18264097	Multiple newly identified loci associated with prostate cancer susceptibility.	Prostate cancer	0	1	1	1
rs11209026	2E-18	17.698970004336	17447842	Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.	Crohn's disease	0	0	1	1
rs13130484	3E-18	17.5228787452803	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs2235544	3E-18	17.5228787452803	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs1250546	3E-18	17.5228787452803	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs17822114	3E-18	17.5228787452803	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs479777	3E-18	17.5228787452803	22837380	A novel sarcoidosis risk locus for Europeans on chromosome 11q13.1.	Sarcoidosis	1	1	1	1
rs1260326	3E-18	17.5228787452803	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Metabolite levels	0	1	1	1
rs559972	3E-18	17.5228787452803	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	0	0
rs6107516	3E-18	17.5228787452803	22137330	Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.	Creutzfeldt-Jakob disease (variant)	0	1	1	1
rs20541	3E-18	17.5228787452803	22075330	A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study.	IgE levels 	1	1	1	1
rs11558471	3E-18	17.5228787452803	21873549	Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.	Proinsulin levels	0	1	1	1
rs12138950	3E-18	17.5228787452803	21565293	Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.	Thyroid volume	0	1	1	1
rs13109457	3E-18	17.5228787452803	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	0	1	1	1
rs7159888	3E-18	17.5228787452803	21203500	Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation.	N-glycan levels	0	1	1	1
rs572169	3E-18	17.5228787452803	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs3136441	3E-18	17.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs2131925	3E-18	17.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs6511720	3E-18	17.5228787452803	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs7501939	3E-18	17.5228787452803	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	1	1	1	1
rs653178	3E-18	17.5228787452803	19430483	Genome-wide association study identifies eight loci associated with blood pressure.	Diastolic blood pressure	0	0	1	1
rs1042725	3E-18	17.5228787452803	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs8034191	3E-18	17.5228787452803	18385676	Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1.	Lung cancer	0	0	1	1
rs16892766	3E-18	17.5228787452803	18372905	A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.	Colorectal cancer	1	1	1	1
rs9292777	3E-18	17.5228787452803	17554261	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.	Crohn's disease	0	0	1	1
rs12708716	3E-18	17.5228787452803	17554260	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs1878528	4E-18	17.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs1933488	4E-18	17.397940008672	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs2516448	4E-18	17.397940008672	23482656	Genome-wide association study of susceptibility loci for cervical cancer.	Cervical cancer	0	1	1	1
rs4821897	4E-18	17.397940008672	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4806073	4E-18	17.397940008672	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	1	1	1	1
rs4766578	4E-18	17.397940008672	22561518	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.	Vitiligo	0	1	1	1
rs11675251	4E-18	17.397940008672	21862451	GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors.	Butyrylcholinesterase levels	1	1	1	1
rs8005161	4E-18	17.397940008672	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	1	1	1	1
rs6651252	4E-18	17.397940008672	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	1	1	1	1
rs1518111	4E-18	17.397940008672	20622878	Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.	Behcet's disease	0	1	1	1
rs1540771	4E-18	17.397940008672	17952075	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Freckles	0	1	1	1
rs9296249	4E-18	17.397940008672	17637780	Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.	Restless legs syndrome	0	0	1	1
rs2145270	5E-18	17.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs11243081	5E-18	17.301029995664	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	1	1	1	1
rs1980057	5E-18	17.301029995664	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs115136538	5E-18	17.301029995664	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	1	1	1	1
rs1701704	5E-18	17.301029995664	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	0	0	0
rs9436640	5E-18	17.301029995664	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs6065906	5E-18	17.301029995664	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	0	0
rs17782313	5E-18	17.301029995664	19079261	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.	Body mass index	0	0	1	1
rs2207790	6E-18	17.2218487496163	23463857	Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.	Electrocardiographic conduction measures	0	1	1	1
rs13144478	6E-18	17.2218487496163	22843503	Genome-wide association analysis identifies TYW3/CRYZ and NDST4 loci associated with circulating resistin levels.	Resistin levels 	1	1	1	1
rs7924176	6E-18	17.2218487496163	21931568	Genome-wide association study identifies four loci associated with eruption of permanent teeth.	Permanent tooth development	1	1	1	1
rs2083637	6E-18	17.2218487496163	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	HDL cholesterol	0	0	0	0
rs17696736	6E-18	17.2218487496163	18978792	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.	Type 1 diabetes	1	1	1	1
rs9268877	6E-18	17.2218487496163	18836448	Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility.	Ulcerative colitis	0	0	1	1
rs1447295	6E-18	17.2218487496163	17401366	Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.	Prostate cancer	0	0	1	1
rs4253252	7E-18	17.1549019599857	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs10488631	7E-18	17.1549019599857	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	0	0	1	1
rs3813582	8E-18	17.0969100130081	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs3925584	8E-18	17.0969100130081	22479191	Genome-wide association and functional follow-up reveals new loci for kidney function.	Chronic kidney disease	1	1	1	1
rs10770705	8E-18	17.0969100130081	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs552976	8E-18	17.0969100130081	20858683	Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.	Glycated hemoglobin levels	0	1	1	1
rs7775698	8E-18	17.0969100130081	19853236	Sequence variants in three loci influence monocyte counts and erythrocyte volume.	Hematology traits	NA	NA	NA	NA
rs4654748	8E-18	17.0969100130081	19303062	Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations.	Folate pathway vitamin levels	0	1	1	1
rs579459	9E-18	17.0457574905607	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs1077989	9E-18	17.0457574905607	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs441460	9E-18	17.0457574905607	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs242557	9E-18	17.0457574905607	21685912	Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.	Progressive supranuclear palsy	0	0	0	0
rs11556924	9E-18	17.0457574905607	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	1	1	1	1
rs6435862	9E-18	17.0457574905607	19412175	Common variations in BARD1 influence susceptibility to high-risk neuroblastoma.	Neuroblastoma (high-risk)	1	1	1	1
rs10182181	1E-17	17	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs7141420	1E-17	17	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	1	1	1	1
rs10088218	1E-17	17	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	0	1	1	1
rs17142067	1E-17	17	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	0	0	0
rs12568930	1E-17	17	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs641153	1E-17	17	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (CNV)	0	1	1	1
rs7528419	1E-17	17	22003152	Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies.	Lipoprotein-associated phospholipase A2 activity and mass	0	0	1	1
rs633185	1E-17	17	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	1	1	1	1
rs17249754	1E-17	17	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	1	1	1	1
rs1063635	1E-17	17	21653640	Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways.	Rheumatoid arthritis	NA	NA	NA	NA
rs964184	1E-17	17	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	1	1	1
rs1011731	1E-17	17	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	1	1	1	1
rs543650	1E-17	17	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs312985	1E-17	17	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs331	1E-17	17	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs628751	1E-17	17	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular hemoglobin	0	1	0	0
rs2523393	1E-17	17	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	0	1	1	1
rs28777	1E-17	17	18483556	A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.	Black vs. blond hair color	0	1	1	1
rs3923809	1E-17	17	17634447	A genetic risk factor for periodic limb movements in sleep.	Restless legs syndrome	0	0	1	1
rs7531118	2E-17	16.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs6472903	2E-17	16.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs8176743	2E-17	16.698970004336	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	0	0	0
rs2816958	2E-17	16.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	1	1	1	1
rs11712066	2E-17	16.698970004336	22306654	Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis.	Infantile hypertrophic pyloric stenosis	1	1	1	1
rs4788815	2E-17	16.698970004336	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Metabolite levels	1	1	1	1
rs560887	2E-17	16.698970004336	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Metabolite levels	0	1	1	1
rs13107325	2E-17	16.698970004336	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	1	1	1	1
rs3087243	2E-17	16.698970004336	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	1	1	1	1
rs174468	2E-17	16.698970004336	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs11209026	2E-17	16.698970004336	21743469	Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.	Ankylosing spondylitis	0	1	1	1
rs1534166	2E-17	16.698970004336	21665994	Genome-wide association study identifies two loci strongly affecting transferrin glycosylation.	Alcohol consumption (transferrin glycosylation)	0	0	0	0
rs6734238	2E-17	16.698970004336	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	1	1	1	1
rs9822268	2E-17	16.698970004336	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs718314	2E-17	16.698970004336	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	1	1	1	1
rs1294421	2E-17	16.698970004336	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	1	1	1	1
rs7138803	2E-17	16.698970004336	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	1	1	1
rs3129109	2E-17	16.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs473902	2E-17	16.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1564348	2E-17	16.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	1	1
rs2816316	2E-17	16.698970004336	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	1	1	1	1
rs1367117	2E-17	16.698970004336	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs1059611	2E-17	16.698970004336	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs2736100	2E-17	16.698970004336	19578367	Genome-wide association study identifies five susceptibility loci for glioma.	Glioma	0	1	1	1
rs12210810	2E-17	16.698970004336	19305409	Common variants at ten loci modulate the QT interval duration in the QTSCD Study.	QT interval	1	1	1	1
rs9594759	2E-17	16.698970004336	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (spine)	0	0	1	1
rs8050136	2E-17	16.698970004336	19056611	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data.	Type 2 diabetes	0	0	1	1
rs6060373	2E-17	16.698970004336	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs28927680	2E-17	16.698970004336	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	Triglycerides	0	0	1	1
rs12463617	3E-17	16.5228787452803	23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Body mass index	0	0	1	1
rs11847263	3E-17	16.5228787452803	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11838472	3E-17	16.5228787452803	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs7164883	3E-17	16.5228787452803	22544366	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	Atrial fibrillation	0	1	1	1
rs199515	3E-17	16.5228787452803	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	1	1	1	1
rs783147	3E-17	16.5228787452803	21900290	Genetic variants, plasma lipoprotein(a) levels, and risk of cardiovascular morbidity and mortality among two prospective cohorts of type 2 diabetes.	Lp (a) levels	1	1	1	1
rs2657879	3E-17	16.5228787452803	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs2075650	3E-17	16.5228787452803	21418511	Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited.	Longevity	0	1	1	1
rs7466269	3E-17	16.5228787452803	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs6029526	3E-17	16.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs1394125	3E-17	16.5228787452803	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs13098911	3E-17	16.5228787452803	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	1	1	1	1
rs2191349	3E-17	16.5228787452803	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	0	0	0
rs7660702	3E-17	16.5228787452803	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	1	1	1
rs1896312	3E-17	16.5228787452803	20062060	Genome-wide association study of PR interval.	PR interval	1	1	1	1
rs2074238	3E-17	16.5228787452803	19305408	Common variants at ten loci influence QT interval duration in the QTGEN Study.	QT interval	1	1	1	1
rs12296050	3E-17	16.5228787452803	19305409	Common variants at ten loci modulate the QT interval duration in the QTSCD Study.	QT interval	1	1	1	1
rs7234864	4E-17	16.397940008672	23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Body mass index	0	0	1	1
rs1318606	4E-17	16.397940008672	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	0	0	0
rs2941484	4E-17	16.397940008672	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs224278	4E-17	16.397940008672	22327514	Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma.	Ewing sarcoma	0	1	1	1
rs6993770	4E-17	16.397940008672	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs2180439	4E-17	16.397940008672	22032556	Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness.	Male-pattern baldness	0	0	1	1
rs1805007	4E-17	16.397940008672	21700618	Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma.	Basal cell carcinoma 	0	1	1	1
rs3760776	4E-17	16.397940008672	21203500	Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation.	N-glycan levels	1	1	1	1
rs780093	4E-17	16.397940008672	20884846	Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.	Urate levels	0	0	1	1
rs9271366	4E-17	16.397940008672	20598377	Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis.	Multiple sclerosis	0	0	1	1
rs6457617	4E-17	16.397940008672	20383147	Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.	Systemic sclerosis	0	0	1	1
rs7561317	4E-17	16.397940008672	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Body mass index	0	0	0	0
rs693	4E-17	16.397940008672	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	LDL cholesterol	0	0	0	0
rs10946808	4E-17	16.397940008672	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	0	0	1	1
rs17321515	4E-17	16.397940008672	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	Triglycerides	0	0	1	1
rs1885486	5E-17	16.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs2030323	5E-17	16.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs2124440	5E-17	16.301029995664	23314186	Genetic variation associated with circulating monocyte count in the eMERGE Network.	Monocyte count	0	1	1	1
rs11710456	5E-17	16.301029995664	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7224610	5E-17	16.301029995664	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs11168048	5E-17	16.301029995664	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	1	1	1	1
rs561722	5E-17	16.301029995664	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	1	1	1	1
rs12980275	5E-17	16.301029995664	22497812	Interleukin 28B polymorphisms are the only common genetic variants associated with low-density lipoprotein cholesterol (LDL-C) in genotype-1 chronic hepatitis C and determine the association between LDL-C and treatment response.	Lipid levels in hepatitis C treatment	0	1	1	1
rs988712	5E-17	16.301029995664	21708048	Genome wide association study identifies KCNMA1 contributing to human obesity.	Obesity	0	0	1	1
rs1768208	5E-17	16.301029995664	21685912	Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.	Progressive supranuclear palsy	1	1	1	1
rs3764650	5E-17	16.301029995664	21460840	Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.	Alzheimer's disease	1	1	1	1
rs11727189	5E-17	16.301029995664	20010835	Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.	Pulmonary function	0	0	1	1
rs492602	5E-17	16.301029995664	18776911	Common variants of FUT2 are associated with plasma vitamin B12 levels.	Vitamin B12 levels	0	1	1	1
rs2542151	5E-17	16.301029995664	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	1	1	1
rs3813582	6E-17	16.2218487496164	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs11710456	6E-17	16.2218487496164	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs798502	6E-17	16.2218487496164	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	0	1	1	1
rs3024505	6E-17	16.2218487496164	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs3197999	6E-17	16.2218487496164	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs2093210	6E-17	16.2218487496164	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1408799	6E-17	16.2218487496164	18488028	Two newly identified genetic determinants of pigmentation in Europeans.	Blue vs. green eyes	1	1	1	1
rs5743289	6E-17	16.2218487496164	17804789	Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.	Crohn's disease	0	0	1	1
rs7652995	7E-17	16.1549019599857	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10821905	7E-17	16.1549019599857	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs2458413	7E-17	16.1549019599857	21623375	Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.	Paget's disease	1	1	1	1
rs12188300	7E-17	16.1549019599857	20953186	Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis.	Psoriatic arthritis	1	1	1	1
rs2638953	7E-17	16.1549019599857	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs7310409	7E-17	16.1549019599857	18439548	Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.	C-reactive protein	0	0	1	1
rs11710456	8E-17	16.0969100130081	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs55791371	8E-17	16.0969100130081	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	0	0	1	1
rs2281845	8E-17	16.0969100130081	21931568	Genome-wide association study identifies four loci associated with eruption of permanent teeth.	Permanent tooth development	1	1	1	1
rs6920220	8E-17	16.0969100130081	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs4712653	8E-17	16.0969100130081	21124317	Integrative genomics identifies LMO1 as a neuroblastoma oncogene.	Neuroblastoma	1	1	1	1
rs9969804	8E-17	16.0969100130081	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs17563	9E-17	16.0457574905607	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (time to first tooth eruption)	1	1	1	1
rs6445035	9E-17	16.0457574905607	23508960	Aspirin hydrolysis in plasma is a variable function of butyrylcholinesterase and platelet-activating factor acetylhydrolase 1b2 (PAFAH1b2).	Aspirin hydrolysis (plasma)	0	1	1	1
rs2186369	9E-17	16.0457574905607	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2945412	9E-17	16.0457574905607	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs541862	9E-17	16.0457574905607	22694956	Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.	Age-related macular degeneration	0	0	1	1
rs4246511	9E-17	16.0457574905607	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs7200786	9E-17	16.0457574905607	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs971074	9E-17	16.0457574905607	21437268	A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium.	Upper aerodigestive tract cancers	1	1	1	1
rs12531711	9E-17	16.0457574905607	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	0	1	1	1
rs1819658	9E-17	16.0457574905607	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	1	1	1	1
rs26868	9E-17	16.0457574905607	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs6017342	9E-17	16.0457574905607	19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Ulcerative colitis	0	0	1	1
rs385893	9E-17	16.0457574905607	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Hematological parameters	0	1	1	1
rs4857855	9E-17	16.0457574905607	19198610	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.	Eosinophil counts	1	1	1	1
rs1490384	1E-16	16	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs7138803	1E-16	16	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs3129871	1E-16	16	23472185	Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.	Multiple sclerosis (OCB status)	0	0	0	0
rs909674	1E-16	16	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2186369	1E-16	16	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs17331332	1E-16	16	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs6716753	1E-16	16	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs6651252	1E-16	16	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	0	0	1	1
rs2266959	1E-16	16	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs10053502	1E-16	16	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs2523722	1E-16	16	22883433	Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia.	Schizophrenia	0	1	1	1
rs1265564	1E-16	16	22293688	1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.	Type 1 diabetes	0	0	1	1
rs1076540	1E-16	16	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs13702	1E-16	16	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	HDL Cholesterol - Triglycerides (HDLC-TG)	0	1	1	1
rs173539	1E-16	16	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	1	1	1
rs2075290	1E-16	16	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Waist Circumference - Triglycerides (WC-TG)	0	1	1	1
rs7134599	1E-16	16	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs17085007	1E-16	16	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs11724635	1E-16	16	21292315	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.	Parkinson's disease	1	1	1	1
rs3197999	1E-16	16	21151127	Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci.	Primary sclerosing cholangitis	0	1	1	1
rs17207986	1E-16	16	20848476	Genetic predictors of medically refractory ulcerative colitis.	Ulcerative colitis	1	1	1	1
rs225717	1E-16	16	21060863	Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo.	Retinal vascular caliber	1	1	1	1
rs33980500	1E-16	16	20953188	Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2.	Psoriasis	0	1	1	1
rs7965584	1E-16	16	20700443	Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.	Magnesium levels	NA	NA	NA	NA
rs1564348	1E-16	16	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs12896399	1E-16	16	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Eye color	0	0	0	0
rs874040	1E-16	16	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	1	1	1	1
rs846111	1E-16	16	19305408	Common variants at ten loci influence QT interval duration in the QTGEN Study.	QT interval	1	1	1	1
rs2395185	1E-16	16	19122664	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.	Ulcerative colitis	0	0	1	1
rs7524102	1E-16	16	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (hip)	0	1	1	1
rs6060369	1E-16	16	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	0	0	1	1
rs2647044	1E-16	16	17632545	A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.	Type 1 diabetes	0	1	1	1
rs9292468	2E-16	15.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs7534091	2E-16	15.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs769449	2E-16	15.698970004336	23562540	GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.	Alzheimer's disease biomarkers	0	0	0	0
rs13329835	2E-16	15.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs2712381	2E-16	15.698970004336	23314186	Genetic variation associated with circulating monocyte count in the eMERGE Network.	Monocyte count	0	1	1	1
rs901683	2E-16	15.698970004336	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs10455872	2E-16	15.698970004336	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity change in response to statin therapy	0	1	1	1
rs2284553	2E-16	15.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs529866	2E-16	15.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs2107595	2E-16	15.698970004336	23041239	Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.	Stroke (ischemic)	1	1	1	1
rs780093	2E-16	15.698970004336	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	1	1	1
rs727428	2E-16	15.698970004336	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Sex hormone-binding globulin levels	0	0	1	1
rs680379	2E-16	15.698970004336	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Sphingolipid levels	1	1	1	1
rs1440581	2E-16	15.698970004336	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Metabolite levels	1	1	1	1
rs1046089	2E-16	15.698970004336	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	0	1	1	1
rs4656784	2E-16	15.698970004336	22075330	A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study.	IgE levels 	0	0	0	0
rs1173771	2E-16	15.698970004336	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	0	1	1	1
rs17367504	2E-16	15.698970004336	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs12258967	2E-16	15.698970004336	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	1	1	1	1
rs4420638	2E-16	15.698970004336	21740922	A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individuals.	Longevity	0	0	1	1
rs740160	2E-16	15.698970004336	21533175	Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.	Dehydroepiandrosterone sulphate levels	0	0	0	0
rs485499	2E-16	15.698970004336	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	0	1	1	1
rs2266788	2E-16	15.698970004336	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Waist Circumference - Triglycerides (WC-TG)	0	0	0	0
rs4510766	2E-16	15.698970004336	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	0	1	1
rs6795735	2E-16	15.698970004336	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	1	1	1	1
rs2287019	2E-16	15.698970004336	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs4986172	2E-16	15.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs6457620	2E-16	15.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs229527	2E-16	15.698970004336	20410501	Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.	Vitiligo	1	1	1	1
rs4607517	2E-16	15.698970004336	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	0	0	0
rs393152	2E-16	15.698970004336	19915575	Genome-wide association study reveals genetic risk underlying Parkinson's disease.	Parkinson's disease	0	0	1	1
rs2736990	2E-16	15.698970004336	19915575	Genome-wide association study reveals genetic risk underlying Parkinson's disease.	Parkinson's disease	0	0	1	1
rs1859962	2E-16	15.698970004336	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	1	1	1	1
rs2075650	2E-16	15.698970004336	19734903	Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease.	Alzheimer's disease	0	0	1	1
rs12708716	2E-16	15.698970004336	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	0	1	1
rs8756	2E-16	15.698970004336	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs6060369	2E-16	15.698970004336	18193045	Common variants in the GDF5-UQCC region are associated with variation in human height.	Height	0	0	1	1
rs6855911	2E-16	15.698970004336	17997608	The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts.	Urate levels	0	0	1	1
rs17696736	2E-16	15.698970004336	17554260	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.	Type 1 diabetes	0	0	1	1
rs424971	3E-16	15.5228787452803	23314186	Genetic variation associated with circulating monocyte count in the eMERGE Network.	Monocyte count	1	1	1	1
rs6770152	3E-16	15.5228787452803	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs6843082	3E-16	15.5228787452803	23041239	Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.	Stroke (ischemic)	0	1	1	1
rs1573036	3E-16	15.5228787452803	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	NA	NA	NA	NA
rs495828	3E-16	15.5228787452803	22672568	A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.	Venous thromboembolism	0	0	1	1
rs2106261	3E-16	15.5228787452803	22544366	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	Atrial fibrillation	1	1	1	1
rs807669	3E-16	15.5228787452803	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Metabolite levels	1	1	1	1
rs1335532	3E-16	15.5228787452803	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs4613763	3E-16	15.5228787452803	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs4242384	3E-16	15.5228787452803	21743057	Genome-wide association study identifies new prostate cancer susceptibility loci.	Prostate cancer	0	0	1	1
rs12982744	3E-16	15.5228787452803	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs10885122	3E-16	15.5228787452803	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	1	1	1	1
rs5753037	3E-16	15.5228787452803	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs10938397	3E-16	15.5228787452803	19079261	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.	Body mass index	0	0	1	1
rs2292239	3E-16	15.5228787452803	18978792	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.	Type 1 diabetes	0	0	1	1
rs11747270	3E-16	15.5228787452803	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs11190140	3E-16	15.5228787452803	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs4242384	3E-16	15.5228787452803	18264097	Multiple newly identified loci associated with prostate cancer susceptibility.	Prostate cancer	0	0	1	1
rs11144688	4E-16	15.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs4535251	4E-16	15.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs2568958	4E-16	15.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs6062509	4E-16	15.397940008672	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	0	1	1	1
rs6828523	4E-16	15.397940008672	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs7652995	4E-16	15.397940008672	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs909674	4E-16	15.397940008672	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs857684	4E-16	15.397940008672	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs4845604	4E-16	15.397940008672	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs923375	4E-16	15.397940008672	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs7559271	4E-16	15.397940008672	22341974	Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position.	Facial morphology	1	1	1	1
rs1023252	4E-16	15.397940008672	21273288	Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster.	Natriuretic peptide levels	0	1	1	1
rs7507204	4E-16	15.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs386000	4E-16	15.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs12566888	4E-16	15.397940008672	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	0	0	0	0
rs2235302	4E-16	15.397940008672	20167578	Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels.	Soluble levels of adhesion molecules	1	1	1	1
rs1532085	4E-16	15.397940008672	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs2062377	4E-16	15.397940008672	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	1	1	1	1
rs314276	4E-16	15.397940008672	19448623	Genetic variation in LIN28B is associated with the timing of puberty.	Menarche (age at onset)	0	0	1	1
rs846111	4E-16	15.397940008672	19305409	Common variants at ten loci modulate the QT interval duration in the QTSCD Study.	QT interval	0	0	1	1
rs4930103	5E-16	15.301029995664	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (parent-of-origin)	1	1	1	1
rs2046210	5E-16	15.301029995664	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	0	0	1	1
rs1063856	5E-16	15.301029995664	23267103	Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.	Coagulation factor levels	1	1	1	1
rs1728918	5E-16	15.301029995664	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	0	1	1	1
rs10830962	5E-16	15.301029995664	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs7200543	5E-16	15.301029995664	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs2157719	5E-16	15.301029995664	21531791	Chromosome 7p11.2 (EGFR) variation influences glioma risk.	Glioma	0	1	1	1
rs173539	5E-16	15.301029995664	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	HDL Cholesterol - Triglycerides (HDLC-TG)	0	1	0	0
rs2155219	5E-16	15.301029995664	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs110419	5E-16	15.301029995664	21124317	Integrative genomics identifies LMO1 as a neuroblastoma oncogene.	Neuroblastoma	1	1	1	1
rs11023787	5E-16	15.301029995664	21104366	A genome-wide association analysis implicates SOX6 as a candidate gene for wrist bone mass.	Wrist bone mass	1	1	1	1
rs181359	5E-16	15.301029995664	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs17318596	5E-16	15.301029995664	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs3925584	5E-16	15.301029995664	20700443	Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.	Magnesium levels	0	1	1	1
rs11221332	5E-16	15.301029995664	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	1	1	1	1
rs12917707	5E-16	15.301029995664	19430482	Multiple loci associated with indices of renal function and chronic kidney disease.	Renal function and chronic kidney disease	0	1	1	1
rs4725982	5E-16	15.301029995664	19305408	Common variants at ten loci influence QT interval duration in the QTGEN Study.	QT interval	1	1	1	1
rs7524102	5E-16	15.301029995664	18445777	Multiple genetic loci for bone mineral density and fractures.	Bone mineral density (hip)	0	0	1	1
rs561241	5E-16	15.301029995664	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Factor VII	0	1	1	1
rs6906287	6E-16	15.2218487496164	23463857	Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.	Electrocardiographic conduction measures	0	1	1	1
rs909674	6E-16	15.2218487496164	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs9310736	6E-16	15.2218487496164	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs6545800	6E-16	15.2218487496164	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs17293632	6E-16	15.2218487496164	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs2015599	6E-16	15.2218487496164	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs9851724	6E-16	15.2218487496164	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs1443512	6E-16	15.2218487496164	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	1	1	1	1
rs1329424	6E-16	15.2218487496164	20385819	Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.	Age-related macular degeneration	0	0	0	0
rs7903146	6E-16	15.2218487496164	19056611	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data.	Type 2 diabetes	0	0	0	0
rs1042725	6E-16	15.2218487496164	17767157	A common variant of HMGA2 is associated with adult and childhood height in the general population.	Height	0	0	1	1
rs1994969	7E-16	15.1549019599857	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (number of teeth)	1	1	1	1
rs2206277	7E-16	15.1549019599857	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs2823093	7E-16	15.1549019599857	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs1864163	7E-16	15.1549019599857	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	0	1	1	1
rs9472138	7E-16	15.1549019599857	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs2186369	7E-16	15.1549019599857	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7294919	7E-16	15.1549019599857	22504417	Identification of common variants associated with human hippocampal and intracranial volumes.	Brain structure	1	1	1	1
rs3129934	7E-16	15.1549019599857	22457343	A genome-wide association study in progressive multiple sclerosis.	Multiple sclerosis	0	0	1	1
rs2248462	7E-16	15.1549019599857	22286212	Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups.	Hodgkin's lymphoma	0	1	1	1
rs932764	7E-16	15.1549019599857	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	1	1	1	1
rs272889	7E-16	15.1549019599857	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs10790162	7E-16	15.1549019599857	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Waist Circumference - Triglycerides (WC-TG)	0	0	0	0
rs17421627	7E-16	15.1549019599857	21060863	Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo.	Retinal vascular caliber	1	1	1	1
rs4282339	7E-16	15.1549019599857	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs274546	7E-16	15.1549019599857	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs4665736	7E-16	15.1549019599857	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs2877716	7E-16	15.1549019599857	20081857	Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.	Two-hour glucose challenge	0	1	1	1
rs4939883	7E-16	15.1549019599857	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	1	1	1
rs7924176	8E-16	15.096910013008	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (number of teeth)	0	1	1	1
rs3791679	8E-16	15.096910013008	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs729761	8E-16	15.096910013008	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs10136766	8E-16	15.096910013008	23225573	Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis.	IgG levels	1	1	1	1
rs9295536	8E-16	15.096910013008	22941191	Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.	Neuroblastoma	0	0	1	1
rs2519093	8E-16	15.096910013008	22672568	A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.	Venous thromboembolism	0	0	0	0
rs2284746	8E-16	15.096910013008	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	1	1	1
rs2968864	8E-16	15.096910013008	19305408	Common variants at ten loci influence QT interval duration in the QTGEN Study.	QT interval	0	0	0	0
rs2271293	8E-16	15.096910013008	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	HDL cholesterol	0	0	1	1
rs2281135	8E-16	15.096910013008	18940312	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.	Liver enzyme levels	0	1	1	1
rs11814448	9E-16	15.0457574905607	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs943080	9E-16	15.0457574905607	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	0	1	1	1
rs10032216	9E-16	15.0457574905607	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs6586030	9E-16	15.0457574905607	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs210142	9E-16	15.0457574905607	22700719	Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.	Chronic lymphocytic leukemia	0	1	1	1
rs4950806	9E-16	15.0457574905607	21862451	GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors.	Butyrylcholinesterase levels	1	1	1	1
rs356220	9E-16	15.0457574905607	21044948	Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.	Parkinson's disease	0	0	1	1
rs889014	9E-16	15.0457574905607	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs4402960	9E-16	15.0457574905607	17463248	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.	Type 2 diabetes	1	1	1	1
rs4402960	9E-16	15.0457574905607	17463249	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs8114671	1E-15	15	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	0	0
rs2280470	1E-15	15	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs16857609	1E-15	15	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs524952	1E-15	15	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs555212	1E-15	15	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	0	0	0
rs516246	1E-15	15	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	0	1	1	1
rs35675666	1E-15	15	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs4839680	1E-15	15	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs999556	1E-15	15	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs2908004	1E-15	15	22792071	WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk.	Bone mineral density	0	0	1	1
rs3736594	1E-15	15	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	1	1	1	1
rs29784	1E-15	15	22306654	Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis.	Infantile hypertrophic pyloric stenosis	1	1	1	1
rs2227831	1E-15	15	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs2571391	1E-15	15	22075330	A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study.	IgE levels 	0	1	1	1
rs281377	1E-15	15	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alkaline phosphatase)	0	1	1	1
rs1327235	1E-15	15	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	1	1	1	1
rs11191593	1E-15	15	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs2236212	1E-15	15	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs9888739	1E-15	15	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	0	0	1	1
rs12239046	1E-15	15	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	1	1	1	1
rs3810936	1E-15	15	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs5742915	1E-15	15	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs7775698	1E-15	15	20927387	A genome-wide association study of red blood cell traits using the electronic medical record.	Red blood cell traits	NA	NA	NA	NA
rs1800961	1E-15	15	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs4731702	1E-15	15	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs1169288	1E-15	15	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	1	1
rs11220462	1E-15	15	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	1	1	1	1
rs5015480	1E-15	15	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	1	1	1	1
rs1847134	1E-15	15	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Eye color	0	1	1	1
rs10206899	1E-15	15	20383145	Genetic loci influencing kidney function and chronic kidney disease.	Creatinine levels	0	1	1	1
rs7422339	1E-15	15	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	NA	NA	NA	NA
rs9895661	1E-15	15	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	0	1	1	1
rs917997	1E-15	15	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs649129	1E-15	15	20167578	Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels.	Soluble levels of adhesion molecules	0	0	0	0
rs172629	1E-15	15	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	0	1	1	1
rs131794	1E-15	15	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	0	1	1	1
rs1256335	1E-15	15	19744961	Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.	Folate pathway vitamin levels	1	1	1	1
rs10821936	1E-15	15	19684603	Germline genomic variants associated with childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	0	0	1	1
rs3087243	1E-15	15	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs2522056	1E-15	15	20031576	Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts.	Fibrinogen	0	1	1	1
rs12576239	1E-15	15	19305408	Common variants at ten loci influence QT interval duration in the QTGEN Study.	QT interval	0	0	1	1
rs10919071	1E-15	15	19305409	Common variants at ten loci modulate the QT interval duration in the QTSCD Study.	QT interval	1	1	1	1
rs1051730	1E-15	15	18978790	Lung cancer susceptibility locus at 5p15.33.	Lung cancer	0	0	1	1
rs910873	1E-15	15	18488026	Common sequence variants on 20q11.22 confer melanoma susceptibility.	Melanoma	1	1	1	1
rs12593813	1E-15	15	17637780	Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.	Restless legs syndrome	0	0	1	1
rs909674	2E-15	14.698970004336	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6671200 	2E-15	14.698970004336	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Stearic acid (18:0) plasma levels	NA	NA	NA	NA
rs6679677	2E-15	14.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	0	1	1	1
rs4246215	2E-15	14.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs1481012	2E-15	14.698970004336	22331829	Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial.	Response to statin therapy (LDL-C)	0	1	1	1
rs17655730	2E-15	14.698970004336	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	0	1	0	0
rs7903146	2E-15	14.698970004336	22101970	Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.	Type 2 diabetes	0	0	1	1
rs10908458	2E-15	14.698970004336	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	0	1	1	1
rs1799945	2E-15	14.698970004336	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	1	1	1	1
rs2521501	2E-15	14.698970004336	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	0	1	0	0
rs633185	2E-15	14.698970004336	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	0	1	0	0
rs1378942	2E-15	14.698970004336	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs669607	2E-15	14.698970004336	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs9621532	2E-15	14.698970004336	21665990	Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.	Age-related macular degeneration	NA	NA	NA	NA
rs855791	2E-15	14.698970004336	21149283	Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.	Iron status biomarkers	0	1	1	1
rs7517810	2E-15	14.698970004336	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs3177928	2E-15	14.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs2247056	2E-15	14.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	1	1
rs12203592	2E-15	14.698970004336	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Eye color	0	1	0	0
rs291671	2E-15	14.698970004336	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Hair color	1	1	1	1
rs2066847	2E-15	14.698970004336	20570966	Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.	Crohn's disease	NA	NA	NA	NA
rs174550	2E-15	14.698970004336	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	1	1	1
rs602662	2E-15	14.698970004336	19744961	Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.	Folate pathway vitamin levels	0	0	1	1
rs2106261	2E-15	14.698970004336	19597492	Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.	Atrial fibrillation	0	0	1	1
rs2968863	2E-15	14.698970004336	19305409	Common variants at ten loci modulate the QT interval duration in the QTSCD Study.	QT interval	0	0	1	1
rs2304130	2E-15	14.698970004336	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	0	1	1
rs7442295	2E-15	14.698970004336	18179892	Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.	Urate levels	0	0	1	1
rs13278062	3E-15	14.5228787452803	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	NA	NA	NA	NA
rs2023472	3E-15	14.5228787452803	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	0	1	1	1
rs13015993	3E-15	14.5228787452803	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs925255	3E-15	14.5228787452803	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs4142248	3E-15	14.5228787452803	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs4806073	3E-15	14.5228787452803	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	0	0	0	0
rs7152623	3E-15	14.5228787452803	22068335	Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium.	Aortic stiffness	1	1	1	1
rs10187424	3E-15	14.5228787452803	21743467	Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.	Prostate cancer	1	1	1	1
rs10790162	3E-15	14.5228787452803	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	HDL Cholesterol - Triglycerides (HDLC-TG)	0	1	0	0
rs798502	3E-15	14.5228787452803	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	0	1	1
rs4809330	3E-15	14.5228787452803	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs9494145	3E-15	14.5228787452803	20927387	A genome-wide association study of red blood cell traits using the electronic medical record.	Red blood cell traits	0	0	1	1
rs243021	3E-15	14.5228787452803	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	1	1	1	1
rs3803662	3E-15	14.5228787452803	20453838	Genome-wide association study identifies five new breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs614367	3E-15	14.5228787452803	20453838	Genome-wide association study identifies five new breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs599839	3E-15	14.5228787452803	20442857	Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study.	Lipoprotein-associated phospholipase A2 activity and mass	0	0	1	1
rs12460876	3E-15	14.5228787452803	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	0	1	1	1
rs1738074	3E-15	14.5228787452803	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	1	1	1	1
rs2070600	3E-15	14.5228787452803	20010834	Genome-wide association study identifies five loci associated with lung function.	Pulmonary function	0	1	1	1
rs9483788	3E-15	14.5228787452803	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hematocrit	0	1	0	0
rs10224002	3E-15	14.5228787452803	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hemoglobin	1	1	1	1
rs4636294	3E-15	14.5228787452803	19578365	Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.	Cutaneous nevi	1	1	1	1
rs7202877	3E-15	14.5228787452803	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs3811647	3E-15	14.5228787452803	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	1	1	1
rs714052	3E-15	14.5228787452803	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	Triglycerides	0	0	1	1
rs3825932	3E-15	14.5228787452803	18978792	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.	Type 1 diabetes	1	1	1	1
rs2180439	3E-15	14.5228787452803	18849994	Susceptibility variants for male-pattern baldness on chromosome 20p11.	Male-pattern baldness	0	0	1	1
rs17782313	3E-15	14.5228787452803	18454148	Common variants near MC4R are associated with fat mass, weight and risk of obesity.	Body mass index	0	0	1	1
rs17788937	4E-15	14.397940008672	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs3803662	4E-15	14.397940008672	23001122	Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk.	Breast cancer (male) 	0	1	1	1
rs560887	4E-15	14.397940008672	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	0	1	1
rs11605924	4E-15	14.397940008672	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	1	1	1	1
rs790356	4E-15	14.397940008672	22544364	A genome-wide association study identifies susceptibility loci for Wilms tumor.	Wilms tumor	1	1	1	1
rs115849089	4E-15	14.397940008672	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	0	0	1	1
rs6900341	4E-15	14.397940008672	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Metabolite levels	0	1	1	1
rs3213545	4E-15	14.397940008672	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	1	1	1
rs3744028	4E-15	14.397940008672	21681796	Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium.	White matter hyperintensity burden	1	1	1	1
rs1610677	4E-15	14.397940008672	21653640	Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways.	Rheumatoid arthritis	0	1	1	1
rs11830103	4E-15	14.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs9398652	4E-15	14.397940008672	20639392	Genome-wide association analysis identifies multiple loci related to resting heart rate.	Resting heart rate	0	1	1	1
rs1063192	4E-15	14.397940008672	20548946	A genome-wide association study of optic disc parameters.	Vertical cup-disc ratio	0	1	1	1
rs9268923	4E-15	14.397940008672	20228798	Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL).	Ulcerative colitis	0	0	1	1
rs10168349	4E-15	14.397940008672	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hematocrit	0	1	1	1
rs17021918	4E-15	14.397940008672	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	1	1	1	1
rs1893217	4E-15	14.397940008672	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs505922	4E-15	14.397940008672	19278955	Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach.	Venous thromboembolism	0	0	1	1
rs1800562	4E-15	14.397940008672	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	1	1	1
rs11082304	5E-15	14.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs1759645	5E-15	14.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs2284746	5E-15	14.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs684232	5E-15	14.301029995664	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs4808801	5E-15	14.301029995664	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs3828840	5E-15	14.301029995664	23472185	Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.	Multiple sclerosis (OCB status)	0	0	0	0
rs3129720	5E-15	14.301029995664	23472185	Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.	Multiple sclerosis (OCB status)	0	0	0	0
rs11045879	5E-15	14.301029995664	23281178	A genome-wide assessment of variability in human serum metabolism.	Metabolite levels	0	1	1	1
rs2235544	5E-15	14.301029995664	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs11847263	5E-15	14.301029995664	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6598541	5E-15	14.301029995664	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs2111485	5E-15	14.301029995664	22561518	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.	Vitiligo	1	1	1	1
rs10455872	5E-15	14.301029995664	22331829	Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial.	Response to statin therapy (LDL-C)	0	1	1	1
rs11075253	5E-15	14.301029995664	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	0	1	1	1
rs17091905	5E-15	14.301029995664	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	1	1	1
rs12670403	5E-15	14.301029995664	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs7307780	5E-15	14.301029995664	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs10788160	5E-15	14.301029995664	21160077	Genetic correction of PSA values using sequence variants associated with PSA levels.	Prostate-specific antigen levels	1	1	1	1
rs2856321	5E-15	14.301029995664	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs429608	5E-15	14.301029995664	20861866	Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs10995190	5E-15	14.301029995664	20453838	Genome-wide association study identifies five new breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs8049607	5E-15	14.301029995664	19305408	Common variants at ten loci influence QT interval duration in the QTGEN Study.	QT interval	1	1	1	1
rs20541	5E-15	14.301029995664	19169254	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.	Psoriasis	0	1	1	1
rs17782313	5E-15	14.301029995664	19151714	Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.	Obesity	0	0	1	1
rs2903492	6E-15	14.2218487496164	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Body mass index	0	0	0	0
rs2943559	6E-15	14.2218487496164	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	0	1	1	1
rs3129871	6E-15	14.2218487496164	23472185	Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.	Multiple sclerosis (OCB status)	0	0	0	0
rs603424	6E-15	14.2218487496164	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	0	1	1	1
rs17694108	6E-15	14.2218487496164	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs1491942	6E-15	14.2218487496164	22438815	Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.	Parkinson's disease	1	1	1	1
rs17608766	6E-15	14.2218487496164	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	1	1	1	1
rs8396	6E-15	14.2218487496164	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs11810217	6E-15	14.2218487496164	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs12203592	6E-15	14.2218487496164	21685912	Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.	Progressive supranuclear palsy	0	1	1	1
rs10224002	6E-15	14.2218487496164	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hematocrit	0	1	0	0
rs16902094	6E-15	14.2218487496164	19767754	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.	Prostate cancer	1	1	1	1
rs4474514	6E-15	14.2218487496164	19483682	Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer.	Testicular cancer	0	1	1	1
rs8049607	6E-15	14.2218487496164	19305409	Common variants at ten loci modulate the QT interval duration in the QTSCD Study.	QT interval	0	0	1	1
rs10748128	7E-15	14.1549019599857	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs2057681	7E-15	14.1549019599857	23281178	A genome-wide assessment of variability in human serum metabolism.	Metabolite levels	0	1	1	1
rs1456896	7E-15	14.1549019599857	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs10882272	7E-15	14.1549019599857	21878437	Genome-wide association study of circulating retinol levels.	Retinol levels	1	1	1	1
rs1738074	7E-15	14.1549019599857	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs227724	7E-15	14.1549019599857	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs7134594	7E-15	14.1549019599857	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs9987289	7E-15	14.1549019599857	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs4908760	7E-15	14.1549019599857	20410501	Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.	Vitiligo	1	1	1	1
rs9883204	7E-15	14.1549019599857	20372150	Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight.	Birth weight	0	0	1	1
rs12899618	7E-15	14.1549019599857	20010834	Genome-wide association study identifies five loci associated with lung function.	Pulmonary function	0	1	1	1
rs4977756	7E-15	14.1549019599857	19578367	Genome-wide association study identifies five susceptibility loci for glioma.	Glioma	0	0	1	1
rs4939883	7E-15	14.1549019599857	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	HDL cholesterol	0	0	1	1
rs1780324	7E-15	14.1549019599857	18940312	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.	Liver enzyme levels	0	1	1	1
rs6469804	7E-15	14.1549019599857	18445777	Multiple genetic loci for bone mineral density and fractures.	Bone mineral density (spine)	0	0	1	1
rs780094	7E-15	14.1549019599857	18439548	Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.	C-reactive protein	0	0	1	1
rs798544	7E-15	14.1549019599857	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs4846914	7E-15	14.1549019599857	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	Triglycerides	0	1	1	1
rs2186369	8E-15	14.096910013008	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10480300	8E-15	14.096910013008	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs13204742	8E-15	14.096910013008	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs10889332	8E-15	14.096910013008	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	1	1	1
rs9303525	8E-15	14.096910013008	22504418	Common variants at 6q22 and 17q21 are associated with intracranial volume.	Intracranial volume	0	1	1	1
rs10199768	8E-15	14.096910013008	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	1	1	1
rs7072216	8E-15	14.096910013008	21931564	A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection.	Metabolite levels	0	0	1	1
rs611744	8E-15	14.096910013008	21732829	Wnt signaling and Dupuytren's disease.	Dupuytren's disease	1	1	1	1
rs11144134	8E-15	14.096910013008	20700443	Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.	Magnesium levels	1	1	1	1
rs1387153	8E-15	14.096910013008	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	0	1	1	1
rs2736100	8E-15	14.096910013008	20543847	Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer.	Testicular germ cell cancer	0	1	1	1
rs680379	8E-15	14.096910013008	19798445	Genetic determinants of circulating sphingolipid concentrations in European populations.	Sphingolipid levels	0	0	1	1
rs10811661	8E-15	14.096910013008	17463248	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.	Type 2 diabetes	1	1	1	1
rs7652995	9E-15	14.0457574905607	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4256159	9E-15	14.0457574905607	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs2517388	9E-15	14.0457574905607	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs17767419	9E-15	14.0457574905607	21565293	Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.	Thyroid volume	0	1	1	1
rs6439167	9E-15	14.0457574905607	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1532085	9E-15	14.0457574905607	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs2315008	9E-15	14.0457574905607	18758464	Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.	Inflammatory bowel disease	0	0	1	1
rs6939340	9E-15	14.0457574905607	18463370	Chromosome 6p22 locus associated with clinically aggressive neuroblastoma.	Neuroblastoma	0	0	1	1
rs4930103	1E-14	14	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	0	1	0	0
rs1074683	1E-14	14	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs11078597	1E-14	14	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	1	1	1	1
rs1851024	1E-14	14	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	1	1	1	1
rs3755132	1E-14	14	22544364	A genome-wide association study identifies susceptibility loci for Wilms tumor.	Wilms tumor	1	1	1	1
rs807624	1E-14	14	22544364	A genome-wide association study identifies susceptibility loci for Wilms tumor.	Wilms tumor	0	0	0	0
rs12051272	1E-14	14	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	0	0	0
rs7841189	1E-14	14	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs9357152	1E-14	14	21896673	Genome-wide association study of HPV seropositivity.	HPV seropositivity	0	1	1	1
rs4648356	1E-14	14	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs10917468	1E-14	14	21565293	Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.	Thyroid volume	0	0	0	0
rs4977756	1E-14	14	21532571	Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.	Glaucoma	0	1	1	1
rs2736100	1E-14	14	21531791	Chromosome 7p11.2 (EGFR) variation influences glioma risk.	Glioma	0	0	1	1
rs1893217	1E-14	14	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs2280470	1E-14	14	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	0	1	1
rs7775698	1E-14	14	20927387	A genome-wide association study of red blood cell traits using the electronic medical record.	Red blood cell traits	NA	NA	NA	NA
rs1169288	1E-14	14	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs4624820	1E-14	14	20543847	Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer.	Testicular germ cell cancer	0	1	1	1
rs11676922	1E-14	14	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	1	1	1	1
rs6420094	1E-14	14	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs8079702	1E-14	14	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (number of teeth)	0	0	0	0
rs11605924	1E-14	14	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	1	1	1
rs10889353	1E-14	14	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	1	1	1
rs331	1E-14	14	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs199533	1E-14	14	19915575	Genome-wide association study reveals genetic risk underlying Parkinson's disease.	Parkinson's disease	0	0	1	1
rs2540917	1E-14	14	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	0	1	1	1
rs11602954	1E-14	14	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	0	0	1	1
rs2200733	1E-14	14	19597491	A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.	Atrial fibrillation	0	0	1	1
rs12053903	1E-14	14	19305408	Common variants at ten loci influence QT interval duration in the QTGEN Study.	QT interval	0	1	1	1
rs1160312	1E-14	14	18849991	Male-pattern baldness susceptibility locus at 20p11.	Male-pattern baldness	0	0	1	1
rs2494250	1E-14	14	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	0	1	1	1
rs11887534	1E-14	14	17632509	A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.	Gallstones	0	1	1	1
rs6983267	1E-14	14	17618284	A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.	Colorectal cancer	0	0	1	1
rs6822844	1E-14	14	17558408	A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.	Celiac disease	0	0	1	1
rs2542151	1E-14	14	17554260	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.	Type 1 diabetes	0	0	1	1
rs1994969	2E-14	13.698970004336	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (time to first tooth eruption)	0	1	0	0
rs7612445	2E-14	13.698970004336	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs2568958	2E-14	13.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Body mass index	0	0	0	0
rs9816226	2E-14	13.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs8008270	2E-14	13.698970004336	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs1432679	2E-14	13.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs975739	2E-14	13.698970004336	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Hair color	1	1	1	1
rs7860634	2E-14	13.698970004336	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs478093	2E-14	13.698970004336	23378610	Genetic variants associated with glycine metabolism and their role in insulin sensitivity and type 2 diabetes.	Metabolite levels	1	1	1	1
rs2186369	2E-14	13.698970004336	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs860873 	2E-14	13.698970004336	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Stearic acid (18:0) plasma levels	NA	NA	NA	NA
rs2077224	2E-14	13.698970004336	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	0	0	0
rs941823	2E-14	13.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs9557195	2E-14	13.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs8005161	2E-14	13.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs445925	2E-14	13.698970004336	23031429	A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol.	Apolipoprotein Levels	0	1	1	1
rs7816345	2E-14	13.698970004336	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs2282679	2E-14	13.698970004336	22673963	Genome-wide association analysis of circulating vitamin D levels in children with asthma.	Vitamin D levels	0	0	1	1
rs11603334	2E-14	13.698970004336	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs7903146	2E-14	13.698970004336	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs2943634	2E-14	13.698970004336	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	0	1	1	1
rs6666258	2E-14	13.698970004336	22544366	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	Atrial fibrillation	0	0	1	1
rs174479	2E-14	13.698970004336	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Sphingolipid levels	0	1	0	0
rs10183486	2E-14	13.698970004336	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs10876550	2E-14	13.698970004336	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs10512472	2E-14	13.698970004336	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs2075650	2E-14	13.698970004336	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	0	1	1
rs4491709	2E-14	13.698970004336	21931568	Genome-wide association study identifies four loci associated with eruption of permanent teeth.	Permanent tooth development	0	1	1	1
rs9393903	2E-14	13.698970004336	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs1990760	2E-14	13.698970004336	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	1	1	1
rs11012732	2E-14	13.698970004336	21804547	Common variation at 10p12.31 near MLLT10 influences meningioma risk.	Meningioma 	1	1	1	1
rs5742915	2E-14	13.698970004336	21623375	Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.	Paget's disease	0	1	1	1
rs12696304	2E-14	13.698970004336	21573004	Genome-wide association study of relative telomere length.	Telomere length	0	0	1	1
rs6687813	2E-14	13.698970004336	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	0	1	1	1
rs610932	2E-14	13.698970004336	21460840	Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.	Alzheimer's disease	1	1	1	1
rs12134279	2E-14	13.698970004336	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	1	1	1	1
rs2075290	2E-14	13.698970004336	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	HDL Cholesterol - Triglycerides (HDLC-TG)	0	0	0	0
rs7608910	2E-14	13.698970004336	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs10495903	2E-14	13.698970004336	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	1	1	1	1
rs3024505	2E-14	13.698970004336	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs2838519	2E-14	13.698970004336	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs1021188	2E-14	13.698970004336	21124946	Genome-wide association meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone.	Bone mineral density	1	1	1	1
rs12534093	2E-14	13.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs7697556	2E-14	13.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs12680655	2E-14	13.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs720390	2E-14	13.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs1351164	2E-14	13.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs634990	2E-14	13.698970004336	20835239	A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14.	Refractive error	0	0	1	1
rs4846914	2E-14	13.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	0	0	0
rs7499892	2E-14	13.698970004336	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs10758658	2E-14	13.698970004336	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular hemoglobin	0	1	0	0
rs10914144	2E-14	13.698970004336	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	0	0	1	1
rs1393350	2E-14	13.698970004336	19578364	Genome-wide association study identifies three loci associated with melanoma risk.	Melanoma	0	1	1	1
rs6441286	2E-14	13.698970004336	19458352	Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.	Primary biliary cirrhosis	0	0	1	1
rs314280	2E-14	13.698970004336	19448622	Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche.	Menarche (age at onset)	0	0	1	1
rs174547	2E-14	13.698970004336	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	Triglycerides	0	0	1	1
rs17696736	2E-14	13.698970004336	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 1 diabetes	0	0	1	1
rs1447295	2E-14	13.698970004336	17401363	Genome-wide association study of prostate cancer identifies a second risk locus at 8q24.	Prostate cancer	0	0	1	1
rs4253399	3E-14	13.5228787452803	23650146	A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Venous thromboembolism	0	1	1	1
rs2941551	3E-14	13.5228787452803	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs1800437	3E-14	13.5228787452803	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs10182181	3E-14	13.5228787452803	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs8170	3E-14	13.5228787452803	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	1	1	1	1
rs10799824	3E-14	13.5228787452803	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs11847263	3E-14	13.5228787452803	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs212388	3E-14	13.5228787452803	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	0	1	1	1
rs2412970	3E-14	13.5228787452803	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs1260326	3E-14	13.5228787452803	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	0	0	0	0
rs2731672	3E-14	13.5228787452803	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	1	1	1
rs13181561	3E-14	13.5228787452803	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs2456973	3E-14	13.5228787452803	22561518	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.	Vitiligo	0	1	1	1
rs117616209	3E-14	13.5228787452803	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Metabolite levels	1	1	1	1
rs1668871	3E-14	13.5228787452803	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	0	0
rs4487645	3E-14	13.5228787452803	22120009	Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.	Multiple myeloma	1	1	1	1
rs13107325	3E-14	13.5228787452803	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	0	1	0	0
rs1458038	3E-14	13.5228787452803	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs17109512	3E-14	13.5228787452803	21900944	Genome-wide association study identifies genetic variants in GOT1 determining serum aspartate aminotransferase levels.	Aspartate aminotransferase 	0	1	1	1
rs477992	3E-14	13.5228787452803	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs7094971	3E-14	13.5228787452803	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs12185268	3E-14	13.5228787452803	21738487	Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.	Parkinson's disease	0	0	1	1
rs12045440	3E-14	13.5228787452803	21565293	Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.	Thyroid volume	1	1	1	1
rs744373	3E-14	13.5228787452803	21460840	Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.	Alzheimer's disease	1	1	1	1
rs6801957	3E-14	13.5228787452803	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	0	1	1	1
rs855791	3E-14	13.5228787452803	20858683	Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.	Glycated hemoglobin levels	0	1	1	1
rs838880	3E-14	13.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs11869286	3E-14	13.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	1	1
rs7349332	3E-14	13.5228787452803	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs1260326	3E-14	13.5228787452803	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	0	1	1	1
rs802734	3E-14	13.5228787452803	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs2070600	3E-14	13.5228787452803	20010835	Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.	Pulmonary function	0	0	1	1
rs331	3E-14	13.5228787452803	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs7679673	3E-14	13.5228787452803	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	1	1	1	1
rs16901979	3E-14	13.5228787452803	19767754	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.	Prostate cancer	1	1	1	1
rs12608932	3E-14	13.5228787452803	19734901	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs1183201	3E-14	13.5228787452803	19503597	Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.	Uric acid levels	0	1	1	1
rs3184504	3E-14	13.5228787452803	19430479	Genome-wide association study of blood pressure and hypertension.	Diastolic blood pressure	0	0	1	1
rs2117032	3E-14	13.5228787452803	19419973	Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.	Bilirubin levels	1	1	1	1
rs780094	3E-14	13.5228787452803	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	Triglycerides	0	0	1	1
rs2144300	3E-14	13.5228787452803	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs7072776	4E-14	13.397940008672	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	0	1	1	1
rs1021188	4E-14	13.397940008672	23437003	Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure.	Bone mineral density	0	0	1	1
rs2721051	4E-14	13.397940008672	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs6863411	4E-14	13.397940008672	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs4728142	4E-14	13.397940008672	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	1	1	1	1
rs7574865	4E-14	13.397940008672	23053960	Genome-wide pathway analysis of genome-wide association studies on systemic lupus erythematosus and rheumatoid arthritis.	Systemic lupus erythematosus	0	0	1	1
rs7587476	4E-14	13.397940008672	22941191	Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.	Neuroblastoma	0	1	1	1
rs11209026	4E-14	13.397940008672	22936669	A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.	Crohn's disease	0	0	1	1
rs2411984	4E-14	13.397940008672	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	1	1	1	1
rs1573036	4E-14	13.397940008672	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	NA	NA	NA	NA
rs1529672	4E-14	13.397940008672	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs6015450	4E-14	13.397940008672	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Hypertension	0	1	0	0
rs1800693	4E-14	13.397940008672	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs3818361	4E-14	13.397940008672	21460840	Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.	Alzheimer's disease	0	1	1	1
rs7561528	4E-14	13.397940008672	21460841	Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.	Alzheimer's disease (late onset)	0	1	1	1
rs579459	4E-14	13.397940008672	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	1	1	1
rs1495741	4E-14	13.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	1	1
rs452036	4E-14	13.397940008672	20639392	Genome-wide association analysis identifies multiple loci related to resting heart rate.	Resting heart rate	0	1	1	1
rs12696304	4E-14	13.397940008672	20139977	Common variants near TERC are associated with mean telomere length.	Telomere length	0	0	1	1
rs2853676	4E-14	13.397940008672	19578367	Genome-wide association study identifies five susceptibility loci for glioma.	Glioma	0	0	0	0
rs2228671	4E-14	13.397940008672	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	LDL cholesterol	0	0	0	0
rs3761847	4E-14	13.397940008672	17804836	TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.	Rheumatoid arthritis	1	1	1	1
rs429358	5E-14	13.301029995664	23419831	APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.	Alzheimer's disease biomarkers	0	0	1	1
rs17084051	5E-14	13.301029995664	23401653	A genome-wide association study for corneal curvature identifies the platelet-derived growth factor receptor α gene as a quantitative trait locus for eye size in white Europeans.	Corneal curvature	1	1	1	1
rs10198628	5E-14	13.301029995664	22589742	Genome-wide association of pericardial fat identifies a unique locus for ectopic fat.	Pericardial fat	1	1	1	1
rs12708716	5E-14	13.301029995664	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	1	1	1
rs9274407	5E-14	13.301029995664	21570397	Susceptibility to amoxicillin-clavulanate-induced liver injury is influenced by multiple HLA class I and II alleles.	Drug-induced liver injury (amoxicillin-clavulanate)	0	1	1	1
rs2470893	5E-14	13.301029995664	21490707	Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.	Caffeine consumption	0	1	1	1
rs2472297	5E-14	13.301029995664	21357676	Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption.	Coffee consumption	0	1	1	1
rs678170	5E-14	13.301029995664	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	NA	NA	NA	NA
rs6556412	5E-14	13.301029995664	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs7849585	5E-14	13.301029995664	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs174548	5E-14	13.301029995664	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs2072590	5E-14	13.301029995664	20852632	A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.	Ovarian cancer	1	1	1	1
rs514230	5E-14	13.301029995664	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	1	1	1	1
rs619865	5E-14	13.301029995664	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Freckling	1	1	1	1
rs13538	5E-14	13.301029995664	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	0	1	1	1
rs8756	5E-14	13.301029995664	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs12210050	5E-14	13.301029995664	19340012	Genome-wide association study of tanning phenotype in a population of European ancestry.	Tanning	1	1	1	1
rs11129795	5E-14	13.301029995664	19305409	Common variants at ten loci modulate the QT interval duration in the QTSCD Study.	QT interval	0	0	1	1
rs1420101	5E-14	13.301029995664	19198610	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.	Eosinophil counts	0	1	1	1
rs3748069	5E-14	13.301029995664	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs864745	5E-14	13.301029995664	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	0	1	1	1
rs10210302	5E-14	13.301029995664	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Crohn's disease	0	0	1	1
rs17817449	6E-14	13.2218487496164	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	0	1	1	1
rs11057841	6E-14	13.2218487496164	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity and mass	1	1	1	1
rs2168889	6E-14	13.2218487496164	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	1	1	1	1
rs603424	6E-14	13.2218487496164	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	0	1	1	1
rs7219669	6E-14	13.2218487496164	22342860	A common variant near the KCNJ2 gene is associated with T-peak to T-end interval.	Cardiac repolarization	1	1	1	1
rs13042885	6E-14	13.2218487496164	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs3731211	6E-14	13.2218487496164	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs1667255	6E-14	13.2218487496164	21878437	Genome-wide association study of circulating retinol levels.	Retinol levels	1	1	1	1
rs16866933	6E-14	13.2218487496164	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs4656461	6E-14	13.2218487496164	21532571	Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.	Glaucoma	1	1	1	1
rs1491942	6E-14	13.2218487496164	21292315	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.	Parkinson's disease	0	0	1	1
rs1079866	6E-14	13.2218487496164	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs1805017	6E-14	13.2218487496164	20442857	Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study.	Lipoprotein-associated phospholipase A2 activity and mass	0	0	1	1
rs4939883	6E-14	13.2218487496164	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs2467853	6E-14	13.2218487496164	19430482	Multiple loci associated with indices of renal function and chronic kidney disease.	Renal function and chronic kidney disease	0	1	1	1
rs6499640	6E-14	13.2218487496164	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	1	1	1	1
rs6859	6E-14	13.2218487496164	18823527	A genome-wide association study for late-onset Alzheimer's disease using DNA pooling.	Alzheimer's disease	1	1	1	1
rs12229918	7E-14	13.1549019599857	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (time to first tooth eruption)	1	1	1	1
rs12203592	7E-14	13.1549019599857	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Non-melanoma skin cancer	0	1	0	0
rs11847263	7E-14	13.1549019599857	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10490924	7E-14	13.1549019599857	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (CNV vs. GA)	0	1	0	0
rs1250544	7E-14	13.1549019599857	22482804	Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.	Crohn's disease and psoriasis	0	1	1	1
rs2950390	7E-14	13.1549019599857	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs11672517	7E-14	13.1549019599857	21732829	Wnt signaling and Dupuytren's disease.	Dupuytren's disease	1	1	1	1
rs13165478	7E-14	13.1549019599857	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs862034	7E-14	13.1549019599857	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs9273349	7E-14	13.1549019599857	20860503	A large-scale, consortium-based genomewide association study of asthma.	Asthma	NA	NA	NA	NA
rs3764261	7E-14	13.1549019599857	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs9373124	7E-14	13.1549019599857	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Other erythrocyte phenotypes	0	0	0	0
rs17300741	7E-14	13.1549019599857	19503597	Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.	Uric acid levels	0	1	1	1
rs8050136	7E-14	13.1549019599857	17463249	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs2076756	7E-14	13.1549019599857	17435756	Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.	Crohn's disease	0	0	1	1
rs1029534	8E-14	13.096910013008	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs872071	8E-14	13.096910013008	22700719	Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.	Chronic lymphocytic leukemia	0	0	1	1
rs3903239	8E-14	13.096910013008	22544366	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	Atrial fibrillation	1	1	1	1
rs13247874	8E-14	13.096910013008	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	0	1	1	1
rs4713103	8E-14	13.096910013008	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs7105934	8E-14	13.096910013008	21131975	Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3.	Renal cell carcinoma	1	1	1	1
rs1514175	8E-14	13.096910013008	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs7971536	8E-14	13.096910013008	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1671152	8E-14	13.096910013008	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	1	1	1	1
rs4744712	8E-14	13.096910013008	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs9859260	8E-14	13.096910013008	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	0	1	1	1
rs365132	8E-14	13.096910013008	19448621	Genome-wide association studies identify loci associated with age at menarche and age at natural menopause.	Menarche and menopause (age at onset)	0	1	1	1
rs1981997	9E-14	13.0457574905607	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	0	1	1	1
rs3764419	9E-14	13.0457574905607	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs476828	9E-14	13.0457574905607	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	0	1	1	1
rs9693444	9E-14	13.0457574905607	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs9358372	9E-14	13.0457574905607	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs2755459	9E-14	13.0457574905607	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	NA	NA	NA	NA
rs12034598	9E-14	13.0457574905607	22291609	A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.	Inflammatory biomarkers	0	1	1	1
rs3026968	9E-14	13.0457574905607	22291609	A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.	Inflammatory biomarkers	1	1	1	1
rs625132	9E-14	13.0457574905607	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs1077667	9E-14	13.0457574905607	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs9894429	9E-14	13.0457574905607	20463881	Digital quantification of human eye color highlights genetic association of three new loci.	Eye color traits	1	1	1	1
rs881858	9E-14	13.0457574905607	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	0	1	1	1
rs11209026	9E-14	13.0457574905607	20062062	Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.	Ankylosing spondylitis	0	0	1	1
rs28777	9E-14	13.0457574905607	18483556	A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.	Black vs. red hair color	0	1	0	0
rs7574865	9E-14	13.0457574905607	18204098	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.	Systemic lupus erythematosus	0	0	1	1
rs2900333	1E-13	13	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	1	1	1	1
rs11895026	1E-13	13	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	1	1	1
rs3101336	1E-13	13	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs3851228	1E-13	13	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs1569723	1E-13	13	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs110419	1E-13	13	22941191	Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.	Neuroblastoma	0	0	1	1
rs673548	1E-13	13	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	1	1	1
rs4780355	1E-13	13	22482804	Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.	Crohn's disease and psoriasis	0	1	1	1
rs1108842	1E-13	13	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	1	1	1	1
rs6947830	1E-13	13	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs479844	1E-13	13	22197932	Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis.	Atopic dermatitis	1	1	1	1
rs10518693	1E-13	13	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs11154801	1E-13	13	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs466639	1E-13	13	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs6438424	1E-13	13	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs10758669	1E-13	13	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs1362212	1E-13	13	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs2019960	1E-13	13	21037568	A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).	Hodgkin's lymphoma	1	1	1	1
rs17716942	1E-13	13	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	0	1	1	1
rs2066807	1E-13	13	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs11648796	1E-13	13	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs11684404	1E-13	13	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs581080	1E-13	13	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs2201841	1E-13	13	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	1	1	1	1
rs7034200	1E-13	13	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	1	1	1	1
rs10889353	1E-13	13	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs16926246	1E-13	13	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hematocrit	0	1	1	1
rs1366594	1E-13	13	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (hip)	0	1	1	1
rs210138	1E-13	13	19483681	A genome-wide association study of testicular germ cell tumor.	Testicular germ cell tumor	0	0	1	1
rs12251307	1E-13	13	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs6088813	1E-13	13	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs4950928	1E-13	13	18403759	Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function.	YKL-40 levels	1	1	1	1
rs1333049	1E-13	13	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Coronary heart disease	0	0	1	1
rs13387042	1E-13	13	17529974	Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer.	Breast cancer	0	0	1	1
rs2241880	1E-13	13	17435756	Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.	Crohn's disease	0	0	1	1
rs6536024	2E-13	12.698970004336	23650146	A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Venous thromboembolism	0	1	1	1
rs10938397	2E-13	12.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Body mass index	0	0	0	0
rs3814333	2E-13	12.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs9816226	2E-13	12.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs12463617	2E-13	12.698970004336	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	0	1	1	1
rs2236007	2E-13	12.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs6504950	2E-13	12.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs7084402	2E-13	12.698970004336	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs10032216	2E-13	12.698970004336	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs11710456	2E-13	12.698970004336	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11847263	2E-13	12.698970004336	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6421315	2E-13	12.698970004336	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs12718598	2E-13	12.698970004336	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs1734907	2E-13	12.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs17229285	2E-13	12.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	1	1	1	1
rs7323755	2E-13	12.698970004336	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs11671010	2E-13	12.698970004336	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	0	0	0	0
rs7910927	2E-13	12.698970004336	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	0	0	0
rs4409785	2E-13	12.698970004336	22561518	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.	Vitiligo	1	1	1	1
rs9926296	2E-13	12.698970004336	22561518	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.	Vitiligo	0	1	1	1
rs4273712	2E-13	12.698970004336	22504418	Common variants at 6q22 and 17q21 are associated with intracranial volume.	Intracranial volume	0	1	1	1
rs2590838	2E-13	12.698970004336	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	0	0	0
rs2954021	2E-13	12.698970004336	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alkaline phosphatase)	0	1	1	1
rs1393350	2E-13	12.698970004336	21983787	Genome-wide association study identifies three new melanoma susceptibility loci.	Melanoma	0	0	1	1
rs7659024	2E-13	12.698970004336	21980494	Genetics of venous thrombosis: insights from a new genome wide association study.	Venous thromboembolism	0	0	1	1
rs419076	2E-13	12.698970004336	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	1	1	1	1
rs17477177	2E-13	12.698970004336	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	1	1	1	1
rs7574865	2E-13	12.698970004336	21750679	Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.	Systemic sclerosis	0	1	1	1
rs2912522	2E-13	12.698970004336	21732829	Wnt signaling and Dupuytren's disease.	Dupuytren's disease	1	1	1	1
rs3091242	2E-13	12.698970004336	21700265	Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate.	Erythrocyte sedimentation rate	1	1	1	1
rs3745516	2E-13	12.698970004336	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	1	1	1	1
rs7524102	2E-13	12.698970004336	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs7554511	2E-13	12.698970004336	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs1398217	2E-13	12.698970004336	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs3180018	2E-13	12.698970004336	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	NA	NA	NA	NA
rs3091315	2E-13	12.698970004336	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs10774625	2E-13	12.698970004336	21060863	Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo.	Retinal vascular caliber	0	1	1	1
rs13107325	2E-13	12.698970004336	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	1	1	1
rs2112347	2E-13	12.698970004336	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	1	1	1
rs1047014	2E-13	12.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs11599750	2E-13	12.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs310405	2E-13	12.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs526896	2E-13	12.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs7027110	2E-13	12.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs10799445	2E-13	12.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2237886	2E-13	12.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1219648	2E-13	12.698970004336	20872241	A combined analysis of genome-wide association studies in breast cancer.	Breast cancer	0	0	1	1
rs1532085	2E-13	12.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	0	0
rs10488631	2E-13	12.698970004336	20383147	Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.	Systemic sclerosis	0	1	1	1
rs2786098	2E-13	12.698970004336	20032318	Variants of DENND1B associated with asthma in children.	Asthma	1	1	1	1
rs2413450	2E-13	12.698970004336	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hematocrit	0	1	0	0
rs12777823	2E-13	12.698970004336	19706858	Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy.	Response to clopidogrel therapy	0	1	1	1
rs17367504	2E-13	12.698970004336	19430483	Genome-wide association study identifies eight loci associated with blood pressure.	Systolic blood pressure	0	1	1	1
rs1393350	2E-13	12.698970004336	19340012	Genome-wide association study of tanning phenotype in a population of European ancestry.	Tanning	0	1	1	1
rs3764147	2E-13	12.698970004336	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs16896068	2E-13	12.698970004336	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs4846914	2E-13	12.698970004336	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	HDL cholesterol	0	0	0	0
rs1805007	2E-13	12.698970004336	17952075	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Blond vs. brown hair color	0	1	0	0
rs995030	3E-13	12.5228787452803	23666239	Meta-analysis identifies four new loci associated with testicular germ cell tumor.	Testicular germ cell tumor	0	0	1	1
rs17796783	3E-13	12.5228787452803	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs7498665	3E-13	12.5228787452803	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs909674	3E-13	12.5228787452803	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2186369	3E-13	12.5228787452803	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1394125	3E-13	12.5228787452803	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs642803	3E-13	12.5228787452803	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs5749446	3E-13	12.5228787452803	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs7657746	3E-13	12.5228787452803	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs1314913	3E-13	12.5228787452803	23001122	Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk.	Breast cancer (male) 	1	1	1	1
rs6679677	3E-13	12.5228787452803	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	0	1	1	1
rs1168029	3E-13	12.5228787452803	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	0	0	1	1
rs4338740	3E-13	12.5228787452803	21565293	Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.	Thyroid volume	1	1	1	1
rs8017161	3E-13	12.5228787452803	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	0	1	1	1
rs3764261	3E-13	12.5228787452803	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	0	0	0
rs9987289	3E-13	12.5228787452803	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	0	1	1	1
rs12817488	3E-13	12.5228787452803	21292315	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.	Parkinson's disease	1	1	1	1
rs7423615	3E-13	12.5228787452803	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs10968576	3E-13	12.5228787452803	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs9360921	3E-13	12.5228787452803	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2110001	3E-13	12.5228787452803	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	NA	NA	NA	NA
rs12474201	3E-13	12.5228787452803	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs231362	3E-13	12.5228787452803	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	1	1	1	1
rs491567	3E-13	12.5228787452803	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs3825214	3E-13	12.5228787452803	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	1	1	1	1
rs11047543	3E-13	12.5228787452803	20062060	Genome-wide association study of PR interval.	PR interval	0	1	1	1
rs1430742	3E-13	12.5228787452803	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	1	1	1	1
rs4624820	3E-13	12.5228787452803	19483681	A genome-wide association study of testicular germ cell tumor.	Testicular germ cell tumor	0	0	1	1
rs314277	3E-13	12.5228787452803	19448621	Genome-wide association studies identify loci associated with age at menarche and age at natural menopause.	Menarche and menopause (age at onset)	0	1	1	1
rs4788084	3E-13	12.5228787452803	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs10795668	3E-13	12.5228787452803	18372905	A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.	Colorectal cancer	1	1	1	1
rs6822844	3E-13	12.5228787452803	18311140	Newly identified genetic risk variants for celiac disease related to the immune response.	Celiac disease	0	0	1	1
rs4420638	3E-13	12.5228787452803	17463246	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	Triglycerides	0	1	1	1
rs1800775	3E-13	12.5228787452803	17463246	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	Triglycerides	0	1	1	1
rs9905704	4E-13	12.397940008672	23666239	Meta-analysis identifies four new loci associated with testicular germ cell tumor.	Testicular germ cell tumor	1	1	1	1
rs10423928	4E-13	12.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs7611694	4E-13	12.397940008672	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs8170	4E-13	12.397940008672	23544013	Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.	Breast Cancer in BRCA1 mutation carriers	0	1	1	1
rs13081855	4E-13	12.397940008672	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	1	1	1	1
rs7616215	4E-13	12.397940008672	23291587	Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.	Behcet's disease	0	1	1	1
rs243070	4E-13	12.397940008672	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs737092	4E-13	12.397940008672	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs4788815	4E-13	12.397940008672	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	0	1	1
rs3757840	4E-13	12.397940008672	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs2307449	4E-13	12.397940008672	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs1260326	4E-13	12.397940008672	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	0	1	1	1
rs11953630	4E-13	12.397940008672	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	1	1	1	1
rs2542151	4E-13	12.397940008672	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	1	1	1
rs4328821	4E-13	12.397940008672	21738480	Multiple loci are associated with white blood cell phenotypes.	White blood cell count	0	1	1	1
rs2517510	4E-13	12.397940008672	21738480	Multiple loci are associated with white blood cell phenotypes.	White blood cell count	1	1	1	1
rs7571971	4E-13	12.397940008672	21685912	Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.	Progressive supranuclear palsy	0	1	1	1
rs798766	4E-13	12.397940008672	20972438	A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.	Bladder cancer	1	1	1	1
rs13129697	4E-13	12.397940008672	20884846	Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.	Urate levels	0	0	0	0
rs3782089	4E-13	12.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs9863706	4E-13	12.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs4072910	4E-13	12.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs4965598	4E-13	12.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2145998	4E-13	12.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs634552	4E-13	12.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs11136341	4E-13	12.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	1	1	1	1
rs1024161	4E-13	12.397940008672	20596022	Genome-wide association study in alopecia areata implicates both innate and adaptive immunity.	Alopecia areata	0	1	1	1
rs13003464	4E-13	12.397940008672	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs9388489	4E-13	12.397940008672	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs1424233	4E-13	12.397940008672	19151714	Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.	Obesity	1	1	1	1
rs6499640	4E-13	12.397940008672	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Body mass index	0	1	0	0
rs174570	4E-13	12.397940008672	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	LDL cholesterol	0	0	1	1
rs10045431	4E-13	12.397940008672	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs5945572	4E-13	12.397940008672	18264098	Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer.	Prostate cancer	NA	NA	NA	NA
rs7517847	4E-13	12.397940008672	17068223	A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.	Inflammatory bowel disease	0	1	1	1
rs9832740	5E-13	12.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs1415701	5E-13	12.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs1993709	5E-13	12.301029995664	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	0	1	1	1
rs1894292	5E-13	12.301029995664	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs12155172	5E-13	12.301029995664	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs10859871	5E-13	12.301029995664	23104006	Genome-wide association meta-analysis identifies new endometriosis risk loci.	Endometriosis	1	1	1	1
rs1998013	5E-13	12.301029995664	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	1	1	1	1
rs2230199	5E-13	12.301029995664	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (GA)	0	1	1	1
rs2295888	5E-13	12.301029995664	22703881	Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.	Prothrombin time	0	1	1	1
rs944002	5E-13	12.301029995664	22010049	Loci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations.	Gamma gluatamyl transferase levels	0	1	1	1
rs4711171	5E-13	12.301029995664	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs10903129	5E-13	12.301029995664	21700265	Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate.	Erythrocyte sedimentation rate	0	0	0	0
rs2266788	5E-13	12.301029995664	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	HDL Cholesterol - Triglycerides (HDLC-TG)	0	0	0	0
rs1994016	5E-13	12.301029995664	21239051	Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies.	Coronary heart disease	0	1	1	1
rs3768716	5E-13	12.301029995664	21124317	Integrative genomics identifies LMO1 as a neuroblastoma oncogene.	Neuroblastoma	0	0	1	1
rs9835332	5E-13	12.301029995664	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs426736	5E-13	12.301029995664	20694013	Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease.	Meningococcal disease	0	1	1	1
rs2642442	5E-13	12.301029995664	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	1	1	1	1
rs12896399	5E-13	12.301029995664	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Hair color	0	0	0	0
rs3018362	5E-13	12.301029995664	20436471	Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.	Paget's disease	0	0	1	1
rs174550	5E-13	12.301029995664	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	0	0	0
rs4939883	5E-13	12.301029995664	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs7775698	5E-13	12.301029995664	19853236	Sequence variants in three loci influence monocyte counts and erythrocyte volume.	Hematology traits	NA	NA	NA	NA
rs12718597	5E-13	12.301029995664	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	0	1	1	1
rs4505848	5E-13	12.301029995664	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs6426833	5E-13	12.301029995664	19122664	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.	Ulcerative colitis	0	0	1	1
rs12970134	5E-13	12.301029995664	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	1	1	1
rs12272004	5E-13	12.301029995664	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	LDL cholesterol	0	0	1	1
rs12272004	5E-13	12.301029995664	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Triglycerides	0	0	0	0
rs4549631	5E-13	12.301029995664	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs8028313	6E-13	12.2218487496164	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs3803662	6E-13	12.2218487496164	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	0	0	1	1
rs1363907	6E-13	12.2218487496164	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs12531711	6E-13	12.2218487496164	23053960	Genome-wide pathway analysis of genome-wide association studies on systemic lupus erythematosus and rheumatoid arthritis.	Systemic lupus erythematosus	0	0	1	1
rs6976053	6E-13	12.2218487496164	22990020	Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation.	Plasminogen activator inhibitor type 1 levels (PAI-1)	0	0	0	0
rs1152591	6E-13	12.2218487496164	22544366	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	Atrial fibrillation	1	1	1	1
rs4241816	6E-13	12.2218487496164	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Metabolite levels	0	1	1	1
rs7068966	6E-13	12.2218487496164	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs1036476	6E-13	12.2218487496164	21909107	Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1.	Thoracic aortic aneurysms and dissections	1	1	1	1
rs17066096	6E-13	12.2218487496164	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs9880192	6E-13	12.2218487496164	21738480	Multiple loci are associated with white blood cell phenotypes.	White blood cell count	0	0	0	0
rs12617311	6E-13	12.2218487496164	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs7927997	6E-13	12.2218487496164	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs13146355	6E-13	12.2218487496164	20700443	Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.	Magnesium levels	0	1	1	1
rs1800961	6E-13	12.2218487496164	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs1561570	6E-13	12.2218487496164	20436471	Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.	Paget's disease	0	0	1	1
rs1751492	6E-13	12.2218487496164	20167575	Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels.	Soluble leptin receptor levels	0	1	1	1
rs12504628	6E-13	12.2218487496164	20010834	Genome-wide association study identifies five loci associated with lung function.	Pulmonary function	0	0	1	1
rs2290400	6E-13	12.2218487496164	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs102275 	7E-13	12.1549019599857	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	NA	NA	NA	NA
rs6496932	7E-13	12.1549019599857	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs11078597	7E-13	12.1549019599857	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	0	0	0	0
rs9389316	7E-13	12.1549019599857	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	1	1	1	1
rs2087160	7E-13	12.1549019599857	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs2518049	7E-13	12.1549019599857	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs494562	7E-13	12.1549019599857	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	1	1	1	1
rs1297265	7E-13	12.1549019599857	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs10993994	7E-13	12.1549019599857	21160077	Genetic correction of PSA values using sequence variants associated with PSA levels.	Prostate-specific antigen levels	0	1	1	1
rs9635759	7E-13	12.1549019599857	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs6473015	7E-13	12.1549019599857	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1558902	7E-13	12.1549019599857	20421936	Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups.	Obesity (extreme)	0	1	1	1
rs3807989	7E-13	12.1549019599857	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	1	1	1
rs10495928	7E-13	12.1549019599857	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hemoglobin	0	1	0	0
rs1000778	7E-13	12.1549019599857	19798445	Genetic determinants of circulating sphingolipid concentrations in European populations.	Sphingolipid levels	0	0	1	1
rs4149056	7E-13	12.1549019599857	19414484	Genome-wide association meta-analysis for total serum bilirubin levels.	Bilirubin levels	0	1	1	1
rs9818870	7E-13	12.1549019599857	19198612	New susceptibility locus for coronary artery disease on chromosome 3q22.3.	Coronary heart disease	1	1	1	1
rs12708716	7E-13	12.1549019599857	18978792	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.	Type 1 diabetes	0	0	1	1
rs2250417	7E-13	12.1549019599857	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs10993994	7E-13	12.1549019599857	18264096	Multiple loci identified in a genome-wide association study of prostate cancer.	Prostate cancer	0	0	1	1
rs17321515	7E-13	12.1549019599857	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs6793295	8E-13	12.0969100130081	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	0	1	1	1
rs2093210	8E-13	12.0969100130081	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs2744971	8E-13	12.0969100130081	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs9915657	8E-13	12.0969100130081	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs4698014	8E-13	12.0969100130081	23703922	A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls.	Uric acid levels	0	0	1	1
rs12103	8E-13	12.0969100130081	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs2488389	8E-13	12.0969100130081	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs419076	8E-13	12.0969100130081	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs10765792	8E-13	12.0969100130081	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs11920090	8E-13	12.0969100130081	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	1	1	1	1
rs11915082	8E-13	12.0969100130081	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular hemoglobin	0	1	0	0
rs7130881	8E-13	12.0969100130081	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	1	1	1	1
rs8170	9E-13	12.0457574905607	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	0	1	1	1
rs112724034	9E-13	12.0457574905607	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs261342	9E-13	12.0457574905607	23281178	A genome-wide assessment of variability in human serum metabolism.	Metabolite levels	0	1	1	1
rs4351	9E-13	12.0457574905607	23281178	A genome-wide assessment of variability in human serum metabolism.	Metabolite levels	0	1	1	1
rs8048576	9E-13	12.0457574905607	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	1	1	1	1
rs11230563	9E-13	12.0457574905607	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs1292053	9E-13	12.0457574905607	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs12678919	9E-13	12.0457574905607	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	1	1	1
rs10521222	9E-13	12.0457574905607	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	1	1	1	1
rs2778031	9E-13	12.0457574905607	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2081687	9E-13	12.0457574905607	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	1	1	1	1
rs3764261	9E-13	12.0457574905607	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs657152	9E-13	12.0457574905607	20529992	Genetic regulation of serum phytosterol levels and risk of coronary artery disease.	Phytosterol levels	0	1	1	1
rs6920220	9E-13	12.0457574905607	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs251253	9E-13	12.0457574905607	20062060	Genome-wide association study of PR interval.	PR interval	0	1	1	1
rs3905000	9E-13	12.0457574905607	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	HDL cholesterol	0	0	1	1
rs2271293	9E-13	12.0457574905607	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	HDL cholesterol	0	0	1	1
rs6983267	9E-13	12.0457574905607	18264097	Multiple newly identified loci associated with prostate cancer susceptibility.	Prostate cancer	0	1	1	1
rs6983267	9E-13	12.0457574905607	17401363	Genome-wide association study of prostate cancer identifies a second risk locus at 8q24.	Prostate cancer	0	0	1	1
rs4826508	1E-12	12	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Zn levels)	NA	NA	NA	NA
rs2350782	1E-12	12	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs572169	1E-12	12	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs2957692	1E-12	12	23381795	Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1.	Circulating vasoactive peptide levels 	1	1	1	1
rs2186369	1E-12	12	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1538138	1E-12	12	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs1178977	1E-12	12	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs259964	1E-12	12	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs727428	1E-12	12	22936694	Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men.	Androgen levels	0	1	1	1
rs1260326	1E-12	12	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	0	1	1
rs9938149	1E-12	12	22814818	Population-based meta-analysis in Caucasians confirms association with COL5A1 and ZNF469 but not COL8A2 with central corneal thickness.	Central corneal thickness	0	0	1	1
rs2230199	1E-12	12	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (CNV)	0	1	0	0
rs10166942	1E-12	12	22683712	Genome-wide association analysis identifies susceptibility loci for migraine without aura.	Migraine	1	1	1	1
rs9287638	1E-12	12	22693459	Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.	Male-pattern baldness	1	1	1	1
rs2073963	1E-12	12	22693459	Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.	Male-pattern baldness	1	1	1	1
rs2157719	1E-12	12	22570617	Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.	Glaucoma (primary open-angle)	0	0	0	0
rs10830963	1E-12	12	22508271	Fasting glucose GWAS candidate region analysis across ethnic groups in the Multiethnic Study of Atherosclerosis (MESA).	Fasting plasma glucose	0	0	1	1
rs10784502	1E-12	12	22504417	Identification of common variants associated with human hippocampal and intracranial volumes.	Brain structure	0	1	1	1
rs2241880	1E-12	12	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	0	0	1	1
rs2297644	1E-12	12	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Metabolite levels	1	1	1	1
rs9834970	1E-12	12	22182935	Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.	Bipolar disorder	1	1	1	1
rs649729	1E-12	12	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	0	1	0	0
rs4420638	1E-12	12	22005931	Genome-wide association analysis of age-at-onset in Alzheimer's disease.	Alzheimer's disease (age of onset)	0	1	1	1
rs7760535	1E-12	12	21886157	Human metabolic individuality in biomedical and pharmaceutical research.	Metabolic traits	0	1	1	1
rs174468	1E-12	12	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs4338740	1E-12	12	21565293	Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.	Thyroid volume	0	0	0	0
rs12190287	1E-12	12	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	1	1	1	1
rs3825807	1E-12	12	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	0	1	1
rs10892279	1E-12	12	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	1	1	1	1
rs3760776	1E-12	12	21203500	Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation.	N-glycan levels	0	0	0	0
rs12720356	1E-12	12	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs422421	1E-12	12	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2336725	1E-12	12	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs855791	1E-12	12	20927387	A genome-wide association study of red blood cell traits using the electronic medical record.	Red blood cell traits	0	0	1	1
rs4820268	1E-12	12	20927387	A genome-wide association study of red blood cell traits using the electronic medical record.	Red blood cell traits	0	0	0	0
rs174548	1E-12	12	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	HDL cholesterol	0	0	0	0
rs3764261	1E-12	12	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	0	0	0
rs16891982	1E-12	12	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Eye color	0	1	0	0
rs267734	1E-12	12	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs9298506	1E-12	12	20364137	Genome-wide association study of intracranial aneurysm identifies three new risk loci.	Intracranial aneurysm	1	1	1	1
rs11661542	1E-12	12	20364137	Genome-wide association study of intracranial aneurysm identifies three new risk loci.	Intracranial aneurysm	1	1	1	1
rs3024493	1E-12	12	20228798	Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL).	Ulcerative colitis	0	0	1	1
rs7034200	1E-12	12	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	0	0	0
rs2571445	1E-12	12	20010834	Genome-wide association study identifies five loci associated with lung function.	Pulmonary function	1	1	1	1
rs10889353	1E-12	12	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs11065987	1E-12	12	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hematocrit	0	1	1	1
rs6932590	1E-12	12	19571808	Common variants conferring risk of schizophrenia.	Schizophrenia	1	1	1	1
rs17319721	1E-12	12	19430482	Multiple loci associated with indices of renal function and chronic kidney disease.	Renal function and chronic kidney disease	0	1	1	1
rs1016988	1E-12	12	20031577	Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.	Fibrinogen	0	0	1	1
rs12970134	1E-12	12	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Body mass index	0	0	0	0
rs2240466	1E-12	12	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Triglycerides	0	0	1	1
rs964184	1E-12	12	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	HDL cholesterol	0	0	0	0
rs3024505	1E-12	12	18836448	Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility.	Ulcerative colitis	0	0	1	1
rs2301436	1E-12	12	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	1	1	1
rs3197999	1E-12	12	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs4939827	1E-12	12	17934461	A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk.	Colorectal cancer	0	0	1	1
rs8050136	1E-12	12	17463248	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.	Type 2 diabetes	0	0	1	1
rs16901979	1E-12	12	17401366	Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.	Prostate cancer	0	0	1	1
rs2194025	2E-12	11.698970004336	23776548	Genetic loci for retinal arteriolar microcirculation.	Retinal arteriolar caliber	0	1	1	1
rs12610495	2E-12	11.698970004336	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	1	1	1	1
rs6882776	2E-12	11.698970004336	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	0	1	1	1
rs11880992	2E-12	11.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs2564921	2E-12	11.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs2025151	2E-12	11.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs4245739	2E-12	11.698970004336	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	1	1	1	1
rs10771399	2E-12	11.698970004336	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	0	0	1	1
rs6762644	2E-12	11.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs2021722	2E-12	11.698970004336	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs2596466	2E-12	11.698970004336	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	1	1	1	1
rs12205363	2E-12	11.698970004336	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs7155454	2E-12	11.698970004336	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs728616	2E-12	11.698970004336	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	0	0	0
rs13126505	2E-12	11.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	0	1	1	1
rs11672691	2E-12	11.698970004336	23065704	A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease.	Prostate cancer	1	1	1	1
rs7077335	2E-12	11.698970004336	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs16861990	2E-12	11.698970004336	22672568	A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.	Venous thromboembolism	0	0	0	0
rs381365	2E-12	11.698970004336	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	NA	NA	NA	NA
rs7771911	2E-12	11.698970004336	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-12p40)	1	1	1	1
rs6048205	2E-12	11.698970004336	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	1	1	1	1
rs1371614	2E-12	11.698970004336	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	1	1	1	1
rs268	2E-12	11.698970004336	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	1	1	1	1
rs2303369	2E-12	11.698970004336	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	0	1	1	1
rs10914144	2E-12	11.698970004336	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	0	0
rs28493229	2E-12	11.698970004336	22081228	Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease.	Kawasaki disease	1	1	1	1
rs1059513	2E-12	11.698970004336	22075330	A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study.	IgE levels 	1	1	1	1
rs12477314	2E-12	11.698970004336	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs2021722	2E-12	11.698970004336	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	0	1	1
rs17398575	2E-12	11.698970004336	21909108	Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.	Carotid intima media thickness	0	1	1	1
rs419076	2E-12	11.698970004336	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	0	1	0	0
rs198846	2E-12	11.698970004336	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs6015450	2E-12	11.698970004336	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs12424086	2E-12	11.698970004336	21931568	Genome-wide association study identifies four loci associated with eruption of permanent teeth.	Permanent tooth development	0	1	1	1
rs3739070	2E-12	11.698970004336	21835309	GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development.	Iris characteristics	1	1	1	1
rs3798713	2E-12	11.698970004336	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs11642873	2E-12	11.698970004336	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	1	1	1
rs12651106	2E-12	11.698970004336	21757653	Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease.	Fibrinogen	1	1	1	1
rs17817449	2E-12	11.698970004336	21552555	A genome-wide association study on obesity and obesity-related traits.	Obesity	0	0	1	1
rs780093	2E-12	11.698970004336	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Waist Circumference - Triglycerides (WC-TG)	0	1	1	1
rs2301271	2E-12	11.698970004336	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	0	0	1	1
rs6589964	2E-12	11.698970004336	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs2058660	2E-12	11.698970004336	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs4871611	2E-12	11.698970004336	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs3817334	2E-12	11.698970004336	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	1	1	1
rs3810291	2E-12	11.698970004336	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs887912	2E-12	11.698970004336	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs6457821	2E-12	11.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs7567288	2E-12	11.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2154319	2E-12	11.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs891088	2E-12	11.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs4601530	2E-12	11.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs6684205	2E-12	11.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs11958779	2E-12	11.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs11118346	2E-12	11.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs2156552	2E-12	11.698970004336	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs1178979	2E-12	11.698970004336	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs3118470	2E-12	11.698970004336	20596022	Genome-wide association study in alopecia areata implicates both innate and adaptive immunity.	Alopecia areata	0	1	1	1
rs4105144	2E-12	11.698970004336	20418888	Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior.	Smoking behavior	NA	NA	NA	NA
rs727957	2E-12	11.698970004336	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	1	1	1	1
rs7189020	2E-12	11.698970004336	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	1	1	1	1
rs7255045	2E-12	11.698970004336	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	1	1	1	1
rs2566755	2E-12	11.698970004336	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (hip)	0	1	0	0
rs4712523	2E-12	11.698970004336	19734900	Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia.	Type 2 diabetes and other traits	0	1	1	1
rs13017599	2E-12	11.698970004336	19503088	REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.	Rheumatoid arthritis	0	1	1	1
rs1465788	2E-12	11.698970004336	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs12917707	2E-12	11.698970004336	19430482	Multiple loci associated with indices of renal function and chronic kidney disease.	Renal function and chronic kidney disease	0	0	0	0
rs1167998	2E-12	11.698970004336	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Triglycerides	0	0	1	1
rs174547	2E-12	11.698970004336	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	HDL cholesterol	0	0	0	0
rs646776	2E-12	11.698970004336	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	LDL cholesterol	0	0	1	1
rs8033165	2E-12	11.698970004336	18483556	A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.	Black vs. red hair color	1	1	1	1
rs3791675	2E-12	11.698970004336	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs7931342	2E-12	11.698970004336	18264097	Multiple newly identified loci associated with prostate cancer susceptibility.	Prostate cancer	0	0	1	1
rs1670533	2E-12	11.698970004336	18239089	Sequence variants in the RNF212 gene associate with genome-wide recombination rate.	Recombination rate (females)	0	1	0	0
rs17145738	2E-12	11.698970004336	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs17234657	2E-12	11.698970004336	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Crohn's disease	0	0	1	1
rs1373692	2E-12	11.698970004336	17447842	Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.	Crohn's disease	0	0	1	1
rs6503905	3E-12	11.5228787452803	23620142	Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.	Circulating myeloperoxidase levels (plasma)	1	1	1	1
rs2307111	3E-12	11.5228787452803	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs10088218	3E-12	11.5228787452803	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	0	0	0	0
rs2535629	3E-12	11.5228787452803	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs271170	3E-12	11.5228787452803	23437003	Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure.	Bone mineral density	1	1	1	1
rs4821897	3E-12	11.5228787452803	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4530903	3E-12	11.5228787452803	23349640	Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.	Lymphoma	0	1	1	1
rs6449213	3E-12	11.5228787452803	23703922	A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls.	Uric acid levels	0	0	0	0
rs3817928	3E-12	11.5228787452803	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs10797432	3E-12	11.5228787452803	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	0	1	1	1
rs3786800	3E-12	11.5228787452803	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs560426	3E-12	11.5228787452803	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs861020	3E-12	11.5228787452803	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs735665	3E-12	11.5228787452803	22700719	Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.	Chronic lymphocytic leukemia	1	1	1	1
rs3184504	3E-12	11.5228787452803	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	0	1	1	1
rs964184	3E-12	11.5228787452803	22437554	Genome-wide association study identifies three common variants associated with serologic response to vitamin E supplementation in men.	Response to Vitamin E supplementation	0	1	1	1
rs11248060	3E-12	11.5228787452803	22438815	Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.	Parkinson's disease	1	1	1	1
rs4731120	3E-12	11.5228787452803	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs4503880	3E-12	11.5228787452803	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs7068966	3E-12	11.5228787452803	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	0	0	0
rs11001819	3E-12	11.5228787452803	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs10468017	3E-12	11.5228787452803	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	1	1	1
rs7129220	3E-12	11.5228787452803	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	0	1	1	1
rs10411936	3E-12	11.5228787452803	21738480	Multiple loci are associated with white blood cell phenotypes.	White blood cell count	1	1	1	1
rs10468017	3E-12	11.5228787452803	21665990	Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.	Age-related macular degeneration	0	1	1	1
rs6421571	3E-12	11.5228787452803	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	0	1	1	1
rs12924729	3E-12	11.5228787452803	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	0	1	1	1
rs2310173	3E-12	11.5228787452803	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	1	1	1	1
rs3760776	3E-12	11.5228787452803	21203500	Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation.	N-glycan levels	0	0	0	0
rs359457	3E-12	11.5228787452803	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	1	1	1	1
rs415890	3E-12	11.5228787452803	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs1738475	3E-12	11.5228787452803	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs8181166	3E-12	11.5228787452803	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs10859563	3E-12	11.5228787452803	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs10761731	3E-12	11.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	1	1
rs4457053	3E-12	11.5228787452803	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	1	1	1	1
rs947583	3E-12	11.5228787452803	20558539	Common genetic variants associate with serum phosphorus concentration.	Phosphorus levels	0	1	1	1
rs869244	3E-12	11.5228787452803	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	1	1	1	1
rs11708067	3E-12	11.5228787452803	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	0	0	0
rs10423928	3E-12	11.5228787452803	20081857	Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.	Two-hour glucose challenge	0	1	1	1
rs3825214	3E-12	11.5228787452803	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	0	0	0
rs1648707	3E-12	11.5228787452803	20011104	A genome-wide association study reveals variants in ARL15 that influence adiponectin levels.	Adiponectin levels	0	0	0	0
rs6010620	3E-12	11.5228787452803	19578367	Genome-wide association study identifies five susceptibility loci for glioma.	Glioma	0	1	1	1
rs6763931	3E-12	11.5228787452803	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs1558744	3E-12	11.5228787452803	19122664	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.	Ulcerative colitis	0	0	1	1
rs5029939	3E-12	11.5228787452803	19165918	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.	Systemic lupus erythematosus	1	1	1	1
rs1393350	3E-12	11.5228787452803	17952075	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Blue vs. green eyes	0	1	1	1
rs7517847	3E-12	11.5228787452803	17435756	Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.	Crohn's disease	0	1	1	1
rs2247056	4E-12	11.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs10058074	4E-12	11.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs12446554	4E-12	11.397940008672	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs16953002	4E-12	11.397940008672	23455637	A variant in FTO shows association with melanoma risk not due to BMI.	Melanoma	1	1	1	1
rs56131196	4E-12	11.397940008672	23419831	APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.	Alzheimer's disease biomarkers	0	0	0	0
rs7837791	4E-12	11.397940008672	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs3138144	4E-12	11.397940008672	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs10065637	4E-12	11.397940008672	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs12663356	4E-12	11.397940008672	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs2382817	4E-12	11.397940008672	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs3774959	4E-12	11.397940008672	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	1	1	1	1
rs1912826	4E-12	11.397940008672	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	0	1	1
rs7944584	4E-12	11.397940008672	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs3807989	4E-12	11.397940008672	22544366	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	Atrial fibrillation	0	1	1	1
rs573872	4E-12	11.397940008672	22306654	Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis.	Infantile hypertrophic pyloric stenosis	1	1	1	1
rs10813766	4E-12	11.397940008672	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs16971217	4E-12	11.397940008672	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	0	1	0	0
rs11616188	4E-12	11.397940008672	21743469	Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.	Ankylosing spondylitis	1	1	1	1
rs2234962	4E-12	11.397940008672	21459883	A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.	Dilated cardiomyopathy	1	1	1	1
rs7665090	4E-12	11.397940008672	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	0	1	1	1
rs941823	4E-12	11.397940008672	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs34372695	4E-12	11.397940008672	21292315	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.	Parkinson's disease	1	1	1	1
rs6599388	4E-12	11.397940008672	21292315	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.	Parkinson's disease	0	0	1	1
rs12153391	4E-12	11.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs10838801	4E-12	11.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	NA	NA	NA	NA
rs750460	4E-12	11.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs6882076	4E-12	11.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	0	0
rs7805747	4E-12	11.397940008672	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	0	1	1	1
rs1558744	4E-12	11.397940008672	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	0	0	1	1
rs4820268	4E-12	11.397940008672	19853236	Sequence variants in three loci influence monocyte counts and erythrocyte volume.	Hematology traits	0	1	1	1
rs219780	4E-12	11.397940008672	19561606	Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.	Kidney stones	1	1	1	1
rs10889353	4E-12	11.397940008672	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	0	0	0
rs7538876	4E-12	11.397940008672	18849993	Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits.	Basal cell carcinoma 	1	1	1	1
rs735665	4E-12	11.397940008672	18758461	A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia.	Chronic lymphocytic leukemia	0	0	1	1
rs2836878	4E-12	11.397940008672	18758464	Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.	Inflammatory bowel disease	0	0	1	1
rs2814993	4E-12	11.397940008672	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs4128725	4E-12	11.397940008672	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	0	0	0	0
rs4888262	5E-12	11.301029995664	23666239	Meta-analysis identifies four new loci associated with testicular germ cell tumor.	Testicular germ cell tumor	1	1	1	1
rs633715	5E-12	11.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Body mass index	0	0	0	0
rs584438	5E-12	11.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs9391253	5E-12	11.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs7498665	5E-12	11.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs10069690	5E-12	11.301029995664	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	0	1	1	1
rs334699	5E-12	11.301029995664	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs16991615	5E-12	11.301029995664	23307926	A genome-wide association study of early menopause and the combined impact of identified variants.	Menopause (age at onset)	0	0	1	1
rs4894535	5E-12	11.301029995664	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	0	1	1	1
rs1007000	5E-12	11.301029995664	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs7044529	5E-12	11.301029995664	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs11618212	5E-12	11.301029995664	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs2283873	5E-12	11.301029995664	22544364	A genome-wide association study identifies susceptibility loci for Wilms tumor.	Wilms tumor	1	1	1	1
rs1800562	5E-12	11.301029995664	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	1	1	1
rs2297909	5E-12	11.301029995664	21743469	Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.	Ankylosing spondylitis	0	1	1	1
rs1893217	5E-12	11.301029995664	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	0	1	1	1
rs2834442	5E-12	11.301029995664	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs965513	5E-12	11.301029995664	20350937	The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl.	Thyroid cancer (Papillary, radiation-related)	0	1	1	1
rs27434	5E-12	11.301029995664	20062062	Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.	Ankylosing spondylitis	0	0	1	1
rs3117582	5E-12	11.301029995664	19836008	A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.	Lung adenocarcinoma	0	1	1	1
rs7781370	5E-12	11.301029995664	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (hip)	1	1	1	1
rs7020673	5E-12	11.301029995664	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs11755527	5E-12	11.301029995664	18978792	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.	Type 1 diabetes	1	1	1	1
rs7176508	5E-12	11.301029995664	18758461	A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia.	Chronic lymphocytic leukemia	1	1	1	1
rs4506565	5E-12	11.301029995664	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 2 diabetes	0	0	1	1
rs13281615	5E-12	11.301029995664	17529967	Genome-wide association study identifies novel breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs1532423	6E-12	11.2218487496164	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Zn levels)	1	1	1	1
rs6141600	6E-12	11.2218487496164	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs10843164	6E-12	11.2218487496164	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs13428823	6E-12	11.2218487496164	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	0	0
rs9472138	6E-12	11.2218487496164	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs11145951	6E-12	11.2218487496164	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	0	1	1	1
rs3931020	6E-12	11.2218487496164	22843503	Genome-wide association analysis identifies TYW3/CRYZ and NDST4 loci associated with circulating resistin levels.	Resistin levels 	1	1	1	1
rs9349379	6E-12	11.2218487496164	22745674	Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis.	Coronary heart disease	0	1	1	1
rs8176719	6E-12	11.2218487496164	22672568	A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.	Venous thromboembolism	0	0	0	0
rs2048161	6E-12	11.2218487496164	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs7173964	6E-12	11.2218487496164	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs17091905	6E-12	11.2218487496164	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	0	0	0
rs1446468	6E-12	11.2218487496164	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	1	1	1	1
rs10166942	6E-12	11.2218487496164	21666692	Genome-wide association study reveals three susceptibility loci for common migraine in the general population.	Migraine	0	0	1	1
rs267939	6E-12	11.2218487496164	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	1	1	1	1
rs4246905	6E-12	11.2218487496164	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs7702331	6E-12	11.2218487496164	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	1	1	1	1
rs6938239	6E-12	11.2218487496164	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	0	1	1
rs4737009	6E-12	11.2218487496164	20858683	Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.	Glycated hemoglobin levels	1	1	1	1
rs2279463	6E-12	11.2218487496164	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs9264942	6E-12	11.2218487496164	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	0	0	0	0
rs9941349	6E-12	11.2218487496164	19553259	Common body mass index-associated variants confer risk of extreme obesity.	Obesity (extreme)	0	0	1	1
rs10946808	6E-12	11.2218487496164	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs2074518	6E-12	11.2218487496164	19305408	Common variants at ten loci influence QT interval duration in the QTGEN Study.	QT interval	1	1	1	1
rs17779747	6E-12	11.2218487496164	19305409	Common variants at ten loci modulate the QT interval duration in the QTSCD Study.	QT interval	0	1	1	1
rs730497	6E-12	11.2218487496164	19096518	Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study.	Glycated hemoglobin levels	0	0	1	1
rs801114	6E-12	11.2218487496164	18849993	Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits.	Basal cell carcinoma 	1	1	1	1
rs3736228	6E-12	11.2218487496164	18455228	Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.	Bone mineral density	1	1	1	1
rs2156552	6E-12	11.2218487496164	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs11805303	6E-12	11.2218487496164	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Crohn's disease	0	0	1	1
rs180242	7E-12	11.1549019599857	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs11154027	7E-12	11.1549019599857	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs12075079	7E-12	11.1549019599857	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs10838798	7E-12	11.1549019599857	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs653178	7E-12	11.1549019599857	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs10500569	7E-12	11.1549019599857	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	1	1	1	1
rs4148441	7E-12	11.1549019599857	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs1878406	7E-12	11.1549019599857	21909108	Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.	Carotid intima media thickness	1	1	1	1
rs10838687	7E-12	11.1549019599857	21873549	Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.	Proinsulin levels	1	1	1	1
rs10875943	7E-12	11.1549019599857	21743467	Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.	Prostate cancer	1	1	1	1
rs17119461	7E-12	11.1549019599857	21706340	A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.	Melanoma	1	1	1	1
rs9939224	7E-12	11.1549019599857	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	0	0	0
rs713875	7E-12	11.1549019599857	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs281379	7E-12	11.1549019599857	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs8070723	7E-12	11.1549019599857	21044948	Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.	Parkinson's disease	0	0	1	1
rs2126259	7E-12	11.1549019599857	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	LDL cholesterol	0	0	1	1
rs11065987	7E-12	11.1549019599857	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	1	1
rs9642880	7E-12	11.1549019599857	20348956	A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.	Urinary bladder cancer	0	1	1	1
rs340874	7E-12	11.1549019599857	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	1	1	1	1
rs6982636	7E-12	11.1549019599857	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	1	1	1
rs11228565	7E-12	11.1549019599857	19767754	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.	Prostate cancer	0	0	1	1
rs29941	7E-12	11.1549019599857	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Body mass index	1	1	1	1
rs744166	7E-12	11.1549019599857	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	1	1	1
rs6983267	7E-12	11.1549019599857	18264096	Multiple loci identified in a genome-wide association study of prostate cancer.	Prostate cancer	0	0	1	1
rs11584700	8E-12	11.0969100130081	23722424	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.	Educational attainment	0	1	1	1
rs506500	8E-12	11.0969100130081	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Se levels)	0	0	0	0
rs13210323	8E-12	11.0969100130081	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs6421315	8E-12	11.0969100130081	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs16909898	8E-12	11.0969100130081	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	1	1	1	1
rs10849023	8E-12	11.0969100130081	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs10495903	8E-12	11.0969100130081	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs9297145	8E-12	11.0969100130081	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs8023580	8E-12	11.0969100130081	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	0	0	0
rs731839	8E-12	11.0969100130081	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	1	1	1	1
rs17610395	8E-12	11.0969100130081	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	NA	NA	NA	NA
rs2153157	8E-12	11.0969100130081	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs7317038	8E-12	11.0969100130081	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs314253	8E-12	11.0969100130081	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alkaline phosphatase)	1	1	1	1
rs1799945	8E-12	11.0969100130081	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	0	1	0	0
rs964184	8E-12	11.0969100130081	21729881	Genome-wide association study identifies common variants associated with circulating vitamin E levels.	Vitamin E levels	0	1	1	1
rs4938933	8E-12	11.0969100130081	21460841	Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.	Alzheimer's disease (late onset)	0	1	1	1
rs11711441	8E-12	11.0969100130081	21292315	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.	Parkinson's disease	1	1	1	1
rs740495	8E-12	11.0969100130081	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs1014971	8E-12	11.0969100130081	20972438	A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.	Bladder cancer	1	1	1	1
rs2629046	8E-12	11.0969100130081	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs3790567	8E-12	11.0969100130081	20639880	Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis.	Primary biliary cirrhosis	1	1	1	1
rs6441286	8E-12	11.0969100130081	20639880	Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis.	Primary biliary cirrhosis	0	0	1	1
rs11066301	8E-12	11.0969100130081	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Hematological parameters	0	1	1	1
rs12772169	8E-12	11.0969100130081	19578179	A genome-wide association study of acenocoumarol maintenance dosage.	Acenocoumarol maintenance dosage	0	1	1	1
rs646776	8E-12	11.0969100130081	19198609	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.	Myocardial infarction (early onset)	0	1	1	1
rs3846663	8E-12	11.0969100130081	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	LDL cholesterol	0	0	1	1
rs8042374	8E-12	11.0969100130081	18978787	Common 5p15.33 and 6p21.33 variants influence lung cancer risk.	Lung cancer	0	0	1	1
rs17024258	9E-12	11.0457574905607	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	1	1	1	1
rs3903072	9E-12	11.0457574905607	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	0	1	1	1
rs1173771	9E-12	11.0457574905607	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	0	1	0	0
rs4902647	9E-12	11.0457574905607	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs1736020	9E-12	11.0457574905607	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs12470505	9E-12	11.0457574905607	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs514230	9E-12	11.0457574905607	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs442177	9E-12	11.0457574905607	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	1	1	1	1
rs2943641	9E-12	11.0457574905607	19734900	Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia.	Type 2 diabetes and other traits	0	1	1	1
rs610604	9E-12	11.0457574905607	19169254	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.	Psoriasis	1	1	1	1
rs7557067	9E-12	11.0457574905607	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	Triglycerides	0	0	1	1
rs9642880	9E-12	11.0457574905607	18794855	Sequence variant on 8q24 confers susceptibility to urinary bladder cancer.	Urinary bladder cancer	0	0	1	1
rs7501939	9E-12	11.0457574905607	18264097	Multiple newly identified loci associated with prostate cancer susceptibility.	Prostate cancer	0	0	1	1
rs2034650	1E-11	11	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	0	1	1	1
rs1950500	1E-11	11	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs11042023	1E-11	11	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	1	1	1	1
rs8028313	1E-11	11	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs72832584	1E-11	11	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs2377339	1E-11	11	23533358	NCK2 is significantly associated with opiates addiction in African-origin men.	Addiction	1	1	1	1
rs10882165	1E-11	11	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs10519227	1E-11	11	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	1	1	1
rs137686	1E-11	11	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6983267	1E-11	11	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	0	0	1	1
rs3851050	1E-11	11	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	1	1	1	1
rs7950726	1E-11	11	23043469	HbA2 levels in normal adults are influenced by two distinct genetic mechanisms.	HbA2 levels	1	1	1	1
rs727428	1E-11	11	22936694	Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men.	Androgen levels	0	0	0	0
rs12051548	1E-11	11	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	1	1	1	1
rs17496332	1E-11	11	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	1	1	1	1
rs12982744	1E-11	11	22566624	Genome-wide association and functional studies identify the DOT1L gene to be involved in cartilage thickness and hip osteoarthritis.	Osteoarthritis	0	1	1	1
rs17606561	1E-11	11	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	0	0	1	1
rs12294104	1E-11	11	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs10852344	1E-11	11	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs9260489	1E-11	11	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	NA	NA	NA	NA
rs11734132	1E-11	11	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs8109288	1E-11	11	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs1719271	1E-11	11	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs13030978	1E-11	11	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs9313772	1E-11	11	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs9309473	1E-11	11	21931564	A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection.	Metabolite levels	0	1	1	1
rs9282641	1E-11	11	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs2546890	1E-11	11	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs7528684	1E-11	11	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	1	1	1	1
rs3129763	1E-11	11	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	1	1	1
rs2524079	1E-11	11	21738480	Multiple loci are associated with white blood cell phenotypes.	White blood cell count	0	0	0	0
rs7040024	1E-11	11	21551455	A second independent locus within DMRT1 is associated with testicular germ cell tumor susceptibility.	Testicular cancer	0	1	1	1
rs860413	1E-11	11	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	1	1	1	1
rs1801239	1E-11	11	21355061	CUBN is a gene locus for albuminuria.	Urinary albumin excretion	1	1	1	1
rs10188217	1E-11	11	21298027	A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease.	Crohn's disease and celiac disease	0	1	1	1
rs1065656	1E-11	11	21216879	A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3.	Insulin-like growth factors	1	1	1	1
rs3739998	1E-11	11	21088011	Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23.	Coronary heart disease	1	1	1	1
rs9491696	1E-11	11	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	0	0	0	0
rs11144688	1E-11	11	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	0	1	1
rs961764	1E-11	11	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs7319045	1E-11	11	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1659127	1E-11	11	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs12916	1E-11	11	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	LDL cholesterol	0	0	1	1
rs10401969	1E-11	11	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	LDL cholesterol	0	0	1	1
rs3757354	1E-11	11	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	1	1	1	1
rs10427255	1E-11	11	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs9469578	1E-11	11	20558539	Common genetic variants associate with serum phosphorus concentration.	Phosphorus levels	1	1	1	1
rs10483727	1E-11	11	20548946	A genome-wide association study of optic disc parameters.	Vertical cup-disc ratio	0	1	1	1
rs6859219	1E-11	11	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs706778	1E-11	11	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs1464510	1E-11	11	20410501	Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.	Vitiligo	0	1	1	1
rs9621532	1E-11	11	20385819	Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.	Age-related macular degeneration	NA	NA	NA	NA
rs798766	1E-11	11	20348956	A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.	Urinary bladder cancer	0	1	1	1
rs9898	1E-11	11	20303064	Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time.	Activated partial thromboplastin time	0	0	1	1
rs7671167	1E-11	11	20173748	Variants in FAM13A are associated with chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease	1	1	1	1
rs2395029	1E-11	11	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	0	0	0	0
rs11168048	1E-11	11	20010835	Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.	Pulmonary function	0	1	1	1
rs331	1E-11	11	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs1408272	1E-11	11	19853236	Sequence variants in three loci influence monocyte counts and erythrocyte volume.	Hematology traits	0	1	1	1
rs11065987	1E-11	11	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hemoglobin	0	1	0	0
rs11085824	1E-11	11	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular hemoglobin	0	1	0	0
rs12500426	1E-11	11	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	0	0	0	0
rs17470137	1E-11	11	19584346	Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.	Aortic root size	1	1	1	1
rs2281808	1E-11	11	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs2568958	1E-11	11	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Body mass index	0	0	1	1
rs1501908	1E-11	11	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	LDL cholesterol	0	0	1	1
rs9467160	1E-11	11	18940312	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.	Liver enzyme levels	0	1	1	1
rs16890979	1E-11	11	18759275	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish.	Uric acid levels	0	0	1	1
rs11584383	1E-11	11	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	1	1	1
rs1812175	1E-11	11	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs1492820	1E-11	11	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	0	0	1	1
rs6931514	1E-11	11	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs4430796	1E-11	11	17603485	Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes.	Prostate cancer	0	0	1	1
rs11171739	1E-11	11	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 1 diabetes	0	0	1	1
rs2609255	2E-11	10.698970004336	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	0	1	1	1
rs987237	2E-11	10.698970004336	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Body mass index	0	0	0	0
rs4245739	2E-11	10.698970004336	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	0	1	1	1
rs11568818	2E-11	10.698970004336	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs3817198	2E-11	10.698970004336	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs603965	2E-11	10.698970004336	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	NA	NA	NA	NA
rs1537370	2E-11	10.698970004336	23561647	Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction.	Coronary artery calcification	0	0	1	1
rs3130783	2E-11	10.698970004336	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	1	1	1	1
rs8135665	2E-11	10.698970004336	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	1	1	1	1
rs1625579	2E-11	10.698970004336	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs7045138	2E-11	10.698970004336	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	NA	NA	NA	NA
rs11158820	2E-11	10.698970004336	23263445	Genetic association suggests that SMOC1 mediates between prenatal sex hormones and digit ratio.	Digit length ratio	1	1	1	1
rs2284746	2E-11	10.698970004336	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs2277027	2E-11	10.698970004336	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	1	1	1	1
rs7068966	2E-11	10.698970004336	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs600550	2E-11	10.698970004336	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity and mass	0	1	1	1
rs3897478	2E-11	10.698970004336	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs872863	2E-11	10.698970004336	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs4561508	2E-11	10.698970004336	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum total protein level	0	0	0	0
rs987525	2E-11	10.698970004336	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	0	0	0	0
rs2071277	2E-11	10.698970004336	22694956	Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.	Age-related macular degeneration	0	1	1	1
rs9292777	2E-11	10.698970004336	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	0	0	1	1
rs13226650	2E-11	10.698970004336	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs11984041	2E-11	10.698970004336	22306652	Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.	Stroke	0	1	1	1
rs2575876	2E-11	10.698970004336	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	0	1	1	1
rs3845624	2E-11	10.698970004336	22291609	A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.	Inflammatory biomarkers	0	0	0	0
rs4305276	2E-11	10.698970004336	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs13072552	2E-11	10.698970004336	22075249	Clinical and genetic association of serum ceruloplasmin with cardiovascular risk.	Serum ceruloplasmin levels	1	1	1	1
rs13962	2E-11	10.698970004336	22075330	A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study.	IgE levels 	NA	NA	NA	NA
rs2865531	2E-11	10.698970004336	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	1	1	1
rs1036429	2E-11	10.698970004336	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs1625579	2E-11	10.698970004336	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	1	1	1
rs11781551	2E-11	10.698970004336	21909108	Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.	Carotid intima media thickness	1	1	1	1
rs805303	2E-11	10.698970004336	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	0	1	1	1
rs11222084	2E-11	10.698970004336	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	1	1	1	1
rs2470893	2E-11	10.698970004336	21876539	Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM.	Coffee consumption	0	0	1	1
rs650258	2E-11	10.698970004336	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs378108	2E-11	10.698970004336	21743469	Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.	Ankylosing spondylitis	0	0	1	1
rs12045440	2E-11	10.698970004336	21565293	Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.	Thyroid volume	0	0	0	0
rs17277546	2E-11	10.698970004336	21533175	Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.	Dehydroepiandrosterone sulphate levels	0	0	0	0
rs911263	2E-11	10.698970004336	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	0	1	1	1
rs6968865	2E-11	10.698970004336	21357676	Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption.	Coffee consumption	0	1	1	1
rs864537	2E-11	10.698970004336	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	1	1	1	1
rs10745954	2E-11	10.698970004336	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	1	1	1	1
rs11067228	2E-11	10.698970004336	21160077	Genetic correction of PSA values using sequence variants associated with PSA levels.	Prostate-specific antigen levels	1	1	1	1
rs212388	2E-11	10.698970004336	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs151181	2E-11	10.698970004336	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs102275	2E-11	10.698970004336	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs8102137	2E-11	10.698970004336	20972438	A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.	Bladder cancer	1	1	1	1
rs8016947	2E-11	10.698970004336	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	1	1	1	1
rs1106766	2E-11	10.698970004336	20884846	Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.	Urate levels	0	0	1	1
rs2247341	2E-11	10.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs17391694	2E-11	10.698970004336	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs964184	2E-11	10.698970004336	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	HDL cholesterol	0	0	0	0
rs2954029	2E-11	10.698970004336	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs4236601	2E-11	10.698970004336	20835238	Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma.	Glaucoma (primary open-angle)	0	1	1	1
rs1835740	2E-11	10.698970004336	20802479	Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.	Migraine	1	1	1	1
rs11220462	2E-11	10.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs2925979	2E-11	10.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	1	1
rs2929282	2E-11	10.698970004336	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	1	1	1	1
rs3093023	2E-11	10.698970004336	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs2957128	2E-11	10.698970004336	20436471	Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.	Paget's disease	0	0	0	0
rs4387287	2E-11	10.698970004336	20421499	Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology.	Telomere length	1	1	1	1
rs1209523	2E-11	10.698970004336	20152958	A weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levels.	Fasting plasma glucose	0	1	1	1
rs10889353	2E-11	10.698970004336	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs4939883	2E-11	10.698970004336	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs6426833	2E-11	10.698970004336	19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Ulcerative colitis	0	0	1	1
rs16926246	2E-11	10.698970004336	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hemoglobin	0	1	0	0
rs8102476	2E-11	10.698970004336	19767754	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.	Prostate cancer	1	1	1	1
rs10852932	2E-11	10.698970004336	19584346	Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.	Aortic root size	1	1	1	1
rs987237	2E-11	10.698970004336	19557161	Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.	Adiposity	0	1	1	1
rs1800693	2E-11	10.698970004336	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs4763879	2E-11	10.698970004336	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs2681472	2E-11	10.698970004336	19430479	Genome-wide association study of blood pressure and hypertension.	Hypertension	0	1	1	1
rs8192284	2E-11	10.698970004336	20031577	Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.	Fibrinogen	NA	NA	NA	NA
rs6756629	2E-11	10.698970004336	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	1	1	1
rs4939883	2E-11	10.698970004336	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	0	1	1
rs4939883	2E-11	10.698970004336	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	HDL cholesterol	0	0	0	0
rs3846662	2E-11	10.698970004336	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	LDL cholesterol	0	0	0	0
rs4870044	2E-11	10.698970004336	18445777	Multiple genetic loci for bone mineral density and fractures.	Bone mineral density (spine)	0	1	1	1
rs12198986	2E-11	10.698970004336	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs10488631	2E-11	10.698970004336	18204098	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.	Systemic lupus erythematosus	0	0	1	1
rs1042602	2E-11	10.698970004336	17952075	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Freckles	0	1	0	0
rs2476601	2E-11	10.698970004336	17804836	TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.	Rheumatoid arthritis	0	0	1	1
rs1990760	2E-11	10.698970004336	17554260	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs1514175	3E-11	10.5228787452803	23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Body mass index	0	0	1	1
rs2856321	3E-11	10.5228787452803	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs13078807	3E-11	10.5228787452803	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	1	1	1	1
rs11780156	3E-11	10.5228787452803	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	0	1	1	1
rs920915	3E-11	10.5228787452803	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs334353	3E-11	10.5228787452803	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	1	1	1	1
rs10455872	3E-11	10.5228787452803	23388002	Genetic associations with valvular calcification and aortic stenosis.	Aortic-valve calcification	0	1	1	1
rs12342831	3E-11	10.5228787452803	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2391388 	3E-11	10.5228787452803	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitic acid (16:0) plasma levels	NA	NA	NA	NA
rs96067	3E-11	10.5228787452803	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs785422	3E-11	10.5228787452803	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs1517352	3E-11	10.5228787452803	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs17119	3E-11	10.5228787452803	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs7521902	3E-11	10.5228787452803	23104006	Genome-wide association meta-analysis identifies new endometriosis risk loci.	Endometriosis	1	1	1	1
rs4336470	3E-11	10.5228787452803	22941191	Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.	Neuroblastoma	0	1	1	1
rs2076530	3E-11	10.5228787452803	22936702	Genome-wide association analysis reveals 12q13.3-q14.1 as new risk locus for sarcoidosis.	Sarcoidosis	0	1	1	1
rs712964	3E-11	10.5228787452803	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	0	1	1
rs4849887	3E-11	10.5228787452803	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs7176508	3E-11	10.5228787452803	22700719	Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.	Chronic lymphocytic leukemia	0	0	1	1
rs17693963	3E-11	10.5228787452803	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	1	1	1	1
rs13111850	3E-11	10.5228787452803	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-10)	1	1	1	1
rs13088281	3E-11	10.5228787452803	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	1	1	1	1
rs7294919	3E-11	10.5228787452803	22504421	Common variants at 12q14 and 12q24 are associated with hippocampal volume.	Hippocampal volume	0	1	1	1
rs2395163	3E-11	10.5228787452803	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	0	1	1	1
rs10830963	3E-11	10.5228787452803	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Metabolite levels	0	1	1	1
rs3000073	3E-11	10.5228787452803	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs12969657	3E-11	10.5228787452803	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs7550918	3E-11	10.5228787452803	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs7641175	3E-11	10.5228787452803	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs6065	3E-11	10.5228787452803	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs6511720	3E-11	10.5228787452803	22003152	Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies.	Lipoprotein-associated phospholipase A2 activity and mass	0	1	1	1
rs805303	3E-11	10.5228787452803	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	0	1	0	0
rs11953630	3E-11	10.5228787452803	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	0	1	0	0
rs2248359	3E-11	10.5228787452803	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs3118470	3E-11	10.5228787452803	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	0	0	0
rs1859962	3E-11	10.5228787452803	21743057	Genome-wide association study identifies new prostate cancer susceptibility loci.	Prostate cancer	0	0	1	1
rs1055129	3E-11	10.5228787452803	21681796	Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium.	White matter hyperintensity burden	0	0	0	0
rs10498635	3E-11	10.5228787452803	21623375	Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.	Paget's disease	1	1	1	1
rs2293370	3E-11	10.5228787452803	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	1	1	1	1
rs301	3E-11	10.5228787452803	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	1	0	0
rs3798220	3E-11	10.5228787452803	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	1	1	1	1
rs1562430	3E-11	10.5228787452803	21263130	Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study.	Breast cancer	0	0	1	1
rs27524	3E-11	10.5228787452803	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	0	1	1	1
rs4823006	3E-11	10.5228787452803	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	1	1	1	1
rs10150332	3E-11	10.5228787452803	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	1	1	1
rs356220	3E-11	10.5228787452803	20711177	Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.	Parkinson's disease	0	0	1	1
rs2072183	3E-11	10.5228787452803	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	1	1	1	1
rs2062375	3E-11	10.5228787452803	20548944	An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.	Osteoporosis	0	1	1	1
rs347685	3E-11	10.5228787452803	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs626277	3E-11	10.5228787452803	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs9543325	3E-11	10.5228787452803	20101243	A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33.	Pancreatic cancer	1	1	1	1
rs11558471	3E-11	10.5228787452803	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	1	1	1
rs7786877	3E-11	10.5228787452803	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	0	1	1	1
rs647316	3E-11	10.5228787452803	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	0	0	1	1
rs3790567	3E-11	10.5228787452803	19458352	Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.	Primary biliary cirrhosis	0	0	1	1
rs425105	3E-11	10.5228787452803	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs849141	3E-11	10.5228787452803	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs693	3E-11	10.5228787452803	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	LDL cholesterol	0	0	1	1
rs2650000	3E-11	10.5228787452803	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	Metabolic traits	0	1	1	1
rs17482753	3E-11	10.5228787452803	20031538	Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions.	HDL cholesterol	0	0	1	1
rs6993813	3E-11	10.5228787452803	18445777	Multiple genetic loci for bone mineral density and fractures.	Bone mineral density (hip)	0	1	0	0
rs2816316	3E-11	10.5228787452803	18311140	Newly identified genetic risk variants for celiac disease related to the immune response.	Celiac disease	0	0	1	1
rs11574637	3E-11	10.5228787452803	18204098	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.	Systemic lupus erythematosus	0	0	1	1
rs6589566	3E-11	10.5228787452803	18179892	Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.	LDL cholesterol	0	0	1	1
rs10505477	3E-11	10.5228787452803	17618283	Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.	Colorectal cancer	0	0	1	1
rs543874	4E-11	10.397940008672	23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Body mass index	0	0	1	1
rs4849887	4E-11	10.397940008672	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	0	1	1	1
rs12896399	4E-11	10.397940008672	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Eye color	0	0	0	0
rs4778879	4E-11	10.397940008672	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs1046089	4E-11	10.397940008672	23307926	A genome-wide association study of early menopause and the combined impact of identified variants.	Menopause (age at onset)	0	0	1	1
rs17632159	4E-11	10.397940008672	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs478607	4E-11	10.397940008672	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs10207392	4E-11	10.397940008672	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs6776003	4E-11	10.397940008672	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs559928	4E-11	10.397940008672	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs10274279	4E-11	10.397940008672	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs445925	4E-11	10.397940008672	23031429	A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol.	Apolipoprotein Levels	0	0	0	0
rs204999	4E-11	10.397940008672	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum total protein level	0	1	1	1
rs7078160	4E-11	10.397940008672	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs10821415	4E-11	10.397940008672	22544366	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	Atrial fibrillation	1	1	1	1
rs10483727	4E-11	10.397940008672	22570617	Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.	Glaucoma (primary open-angle)	0	1	1	1
rs7342306	4E-11	10.397940008672	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	0	0
rs12145922	4E-11	10.397940008672	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs2943650	4E-11	10.397940008672	21706003	Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.	Adiposity	0	1	1	1
rs1411478	4E-11	10.397940008672	21685912	Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.	Progressive supranuclear palsy	1	1	1	1
rs1562990	4E-11	10.397940008672	21627779	The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease.	Alzheimer's disease	0	0	1	1
rs1953126	4E-11	10.397940008672	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	0	1	1	1
rs4820268	4E-11	10.397940008672	21208937	Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.	Iron levels	0	1	1	1
rs10980926	4E-11	10.397940008672	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs1799964	4E-11	10.397940008672	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs13333226	4E-11	10.397940008672	21082022	Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension.	Hypertension	0	1	1	1
rs1495741	4E-11	10.397940008672	20972438	A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.	Bladder cancer	0	1	1	1
rs2294008	4E-11	10.397940008672	20972438	A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.	Bladder cancer	1	1	1	1
rs12720356	4E-11	10.397940008672	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	0	1	1	1
rs4795067	4E-11	10.397940008672	20953189	Genome-wide association analysis identifies three psoriasis susceptibility loci.	Psoriasis	1	1	1	1
rs13078807	4E-11	10.397940008672	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	1	1	1
rs17782313	4E-11	10.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs10010325	4E-11	10.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs654723	4E-11	10.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs17081935	4E-11	10.397940008672	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1387153	4E-11	10.397940008672	20858683	Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.	Glycated hemoglobin levels	0	1	1	1
rs12027135	4E-11	10.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	1	1
rs2072183	4E-11	10.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs8017377	4E-11	10.397940008672	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	1	1	1	1
rs10488631	4E-11	10.397940008672	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs653178	4E-11	10.397940008672	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	0	1	1	1
rs4654748	4E-11	10.397940008672	19744961	Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.	Folate pathway vitamin levels	0	0	1	1
rs2681492	4E-11	10.397940008672	19430479	Genome-wide association study of blood pressure and hypertension.	Systolic blood pressure	0	1	0	0
rs6570507	4E-11	10.397940008672	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs6919346	4E-11	10.397940008672	19124843	Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q.	Lp (a) levels	1	1	1	1
rs1800562	4E-11	10.397940008672	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	0	0	0
rs17216525	4E-11	10.397940008672	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	Triglycerides	0	0	1	1
rs4820599	4E-11	10.397940008672	18940312	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.	Liver enzyme levels	0	1	1	1
rs1038304	4E-11	10.397940008672	18445777	Multiple genetic loci for bone mineral density and fractures.	Bone mineral density (spine)	0	0	0	0
rs10512248	4E-11	10.397940008672	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	1	1	1
rs12735613	4E-11	10.397940008672	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs11206510	4E-11	10.397940008672	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	LDL cholesterol	1	1	1	1
rs17221417	4E-11	10.397940008672	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Crohn's disease	0	0	1	1
rs7754840	4E-11	10.397940008672	17463246	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	Type 2 diabetes	0	0	1	1
rs7754840	4E-11	10.397940008672	17463248	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.	Type 2 diabetes	0	0	1	1
rs11209026	4E-11	10.397940008672	17068223	A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.	Inflammatory bowel disease	0	0	1	1
rs4851266	5E-11	10.301029995664	23722424	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.	Educational attainment	0	1	1	1
rs10948222	5E-11	10.301029995664	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs2072590	5E-11	10.301029995664	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	0	0	1	1
rs1881492	5E-11	10.301029995664	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs3780486	5E-11	10.301029995664	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs17482078	5E-11	10.301029995664	23291587	Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.	Behcet's disease	0	1	1	1
rs2869967	5E-11	10.301029995664	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs7594321	5E-11	10.301029995664	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	1	1	1	1
rs724577	5E-11	10.301029995664	23202124	New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.	Birth weight	0	1	1	1
rs17178006	5E-11	10.301029995664	22504421	Common variants at 12q14 and 12q24 are associated with hippocampal volume.	Hippocampal volume	1	1	1	1
rs6532194	5E-11	10.301029995664	22438815	Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.	Parkinson's disease	1	1	1	1
rs116909374	5E-11	10.301029995664	22267200	Discovery of common variants associated with low TSH levels and thyroid cancer risk.	Thyroid cancer	1	1	1	1
rs944002	5E-11	10.301029995664	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	0	1	1	1
rs11082304	5E-11	10.301029995664	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs6511720	5E-11	10.301029995664	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	1	1	1
rs633185	5E-11	10.301029995664	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Hypertension	0	1	0	0
rs4373814	5E-11	10.301029995664	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	1	1	1	1
rs7595037	5E-11	10.301029995664	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs1321535	5E-11	10.301029995664	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs498872	5E-11	10.301029995664	21531791	Chromosome 7p11.2 (EGFR) variation influences glioma risk.	Glioma	0	1	1	1
rs7181230	5E-11	10.301029995664	21533175	Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.	Dehydroepiandrosterone sulphate levels	1	1	1	1
rs11117432	5E-11	10.301029995664	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	0	1	1	1
rs10830956	5E-11	10.301029995664	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	1	1	1
rs2872507	5E-11	10.301029995664	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs780093	5E-11	10.301029995664	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs3213094	5E-11	10.301029995664	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	0	0	1	1
rs2814982	5E-11	10.301029995664	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	1	1
rs4805834	5E-11	10.301029995664	20383145	Genetic loci influencing kidney function and chronic kidney disease.	Creatinine levels	0	1	1	1
rs13010713	5E-11	10.301029995664	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	1	1	1	1
rs4844096	5E-11	10.301029995664	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (number of teeth)	NA	NA	NA	NA
rs3807375	5E-11	10.301029995664	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	1	1	1
rs11897119	5E-11	10.301029995664	20062060	Genome-wide association study of PR interval.	PR interval	0	1	1	1
rs6457327	5E-11	10.301029995664	19620980	Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma.	Follicular lymphoma	0	1	1	1
rs703842	5E-11	10.301029995664	19525955	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.	Multiple sclerosis	1	1	1	1
rs7498665	5E-11	10.301029995664	19079261	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.	Body mass index	0	0	1	1
rs6625163	5E-11	10.301029995664	18849991	Male-pattern baldness susceptibility locus at 20p11.	Male-pattern baldness	NA	NA	NA	NA
rs8033165	5E-11	10.301029995664	18483556	A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.	Black vs. blond hair color	0	1	0	0
rs5215	5E-11	10.301029995664	17463249	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.	Type 2 diabetes	1	1	1	1
rs17101923	6E-11	10.2218487496164	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (time to first tooth eruption)	0	1	1	1
rs2030323	6E-11	10.2218487496164	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs3814113	6E-11	10.2218487496164	23544013	Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.	Ovarian cancer in BRCA1 mutation carriers 	0	1	1	1
rs58370486	6E-11	10.2218487496164	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs493014:rs886090	6E-11	10.2218487496164	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs9275563	6E-11	10.2218487496164	23472185	Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.	Multiple sclerosis (OCB status)	0	0	0	0
rs11710456	6E-11	10.2218487496164	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2307121	6E-11	10.2218487496164	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs11104870	6E-11	10.2218487496164	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs670523	6E-11	10.2218487496164	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs1042058	6E-11	10.2218487496164	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs12173570	6E-11	10.2218487496164	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	0	1	1	1
rs7766070	6E-11	10.2218487496164	22693455	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.	Type 2 diabetes	0	0	1	1
rs7561528	6E-11	10.2218487496164	22832961	Genome-wide association study of Alzheimer's disease.	Alzheimer's disease	0	0	1	1
rs10513686	6E-11	10.2218487496164	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	0	1	1	1
rs539514	6E-11	10.2218487496164	21980299	A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.	Type 1 diabetes	1	1	1	1
rs3756008	6E-11	10.2218487496164	21980494	Genetics of venous thrombosis: insights from a new genome wide association study.	Venous thromboembolism	0	0	1	1
rs12037222	6E-11	10.2218487496164	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	1	1	1	1
rs2838519	6E-11	10.2218487496164	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs4430796	6E-11	10.2218487496164	21160077	Genetic correction of PSA values using sequence variants associated with PSA levels.	Prostate-specific antigen levels	0	1	1	1
rs11847697	6E-11	10.2218487496164	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs2902940	6E-11	10.2218487496164	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	1	1	1	1
rs2293889	6E-11	10.2218487496164	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs2642442	6E-11	10.2218487496164	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs10871777	6E-11	10.2218487496164	20421936	Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups.	Obesity (extreme)	0	1	1	1
rs5936487	6E-11	10.2218487496164	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (time to first tooth eruption)	NA	NA	NA	NA
rs2504063	6E-11	10.2218487496164	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	1	1	1	1
rs1172822	6E-11	10.2218487496164	19448619	Loci at chromosomes 13, 19 and 20 influence age at natural menopause.	Menopause (age at onset)	0	0	1	1
rs9982601	6E-11	10.2218487496164	19198609	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.	Myocardial infarction (early onset)	0	1	1	1
rs7395662	6E-11	10.2218487496164	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	HDL cholesterol	0	1	1	1
rs3791679	6E-11	10.2218487496164	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs10492321	7E-11	10.1549019599857	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs9420907	7E-11	10.1549019599857	23535734	Identification of seven loci affecting mean telomere length and their association with disease.	Telomere length	0	0	1	1
rs1270884	7E-11	10.1549019599857	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs720475	7E-11	10.1549019599857	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs11023139	7E-11	10.1549019599857	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs4698775	7E-11	10.1549019599857	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	1	1	1	1
rs2969180	7E-11	10.1549019599857	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs17348299	7E-11	10.1549019599857	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6421315	7E-11	10.1549019599857	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1529672	7E-11	10.1549019599857	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs1532085	7E-11	10.1549019599857	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs12220777	7E-11	10.1549019599857	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	0	0	0
rs11672983	7E-11	10.1549019599857	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs3790455	7E-11	10.1549019599857	22683712	Genome-wide association analysis identifies susceptibility loci for migraine without aura.	Migraine	1	1	1	1
rs6581612	7E-11	10.1549019599857	22504421	Common variants at 12q14 and 12q24 are associated with hippocampal volume.	Hippocampal volume	0	0	0	0
rs4666002	7E-11	10.1549019599857	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	0	1	1	1
rs7228085	7E-11	10.1549019599857	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	0	0	1	1
rs1801274	7E-11	10.1549019599857	22081228	Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease.	Kawasaki disease	0	1	1	1
rs10235789	7E-11	10.1549019599857	21835309	GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development.	Iris characteristics	1	1	1	1
rs561655	7E-11	10.1549019599857	21460841	Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.	Alzheimer's disease (late onset)	1	1	1	1
rs10874746	7E-11	10.1549019599857	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs7652177	7E-11	10.1549019599857	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	0	1	1
rs13107325	7E-11	10.1549019599857	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	1	1
rs7647305	7E-11	10.1549019599857	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Body mass index	0	0	1	1
rs7679	7E-11	10.1549019599857	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	Triglycerides	0	0	1	1
rs11209026	7E-11	10.1549019599857	18758464	Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.	Inflammatory bowel disease	0	0	1	1
rs6983267	7E-11	10.1549019599857	18372905	A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.	Colorectal cancer	0	0	1	1
rs2903692	7E-11	10.1549019599857	17632545	A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.	Type 1 diabetes	0	0	1	1
rs10033464	7E-11	10.1549019599857	17603472	Variants conferring risk of atrial fibrillation on chromosome 4q25.	Atrial fibrillation/atrial flutter	0	0	0	0
rs5219	7E-11	10.1549019599857	17463248	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.	Type 2 diabetes	0	0	1	1
rs11135910	8E-11	10.096910013008	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs603965	8E-11	10.096910013008	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	NA	NA	NA	NA
rs1656404	8E-11	10.096910013008	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	0	0	0	0
rs13015993	8E-11	10.096910013008	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs11065987	8E-11	10.096910013008	23297363	Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.	Tetralogy of Fallot	0	1	1	1
rs17616316	8E-11	10.096910013008	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs12525668	8E-11	10.096910013008	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs11920090	8E-11	10.096910013008	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs4938642	8E-11	10.096910013008	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs964184	8E-11	10.096910013008	22003152	Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies.	Lipoprotein-associated phospholipase A2 activity and mass	0	1	1	1
rs11191548	8E-11	10.096910013008	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	0	0	0
rs17674580	8E-11	10.096910013008	21750109	European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.	Bladder cancer	1	1	1	1
rs7758128	8E-11	10.096910013008	21326295	Genome-wide analysis identifies a quantitative trait locus in the MHC class II region associated with generalized vitiligo age of onset.	Vitiligo	1	1	1	1
rs4676406	8E-11	10.096910013008	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs4415084	8E-11	10.096910013008	21263130	Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study.	Breast cancer	0	0	1	1
rs3745516	8E-11	10.096910013008	20639880	Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis.	Primary biliary cirrhosis	0	0	1	1
rs12296050	8E-11	10.096910013008	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	1	1	1
rs6136489	8E-11	10.096910013008	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	0	0	1	1
rs11978267	8E-11	10.096910013008	19684603	Germline genomic variants associated with childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	0	0	1	1
rs891835	8E-11	10.096910013008	19578367	Genome-wide association study identifies five susceptibility loci for glioma.	Glioma	0	0	0	0
rs1776897	8E-11	10.096910013008	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs10512597	8E-11	10.096910013008	20031577	Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.	Fibrinogen	1	1	1	1
rs13147758	8E-11	10.096910013008	19300500	A genome-wide association study of pulmonary function measures in the Framingham Heart Study.	Pulmonary function	0	0	1	1
rs3087243	8E-11	10.096910013008	18978792	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.	Type 1 diabetes	0	0	1	1
rs3821236	8E-11	10.096910013008	19165918	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.	Systemic lupus erythematosus	0	0	1	1
rs8017304	9E-11	10.0457574905607	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	0	1	1	1
rs4788196	9E-11	10.0457574905607	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	1	1	1	1
rs17723470	9E-11	10.0457574905607	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs3780486	9E-11	10.0457574905607	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7495132	9E-11	10.0457574905607	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs9419958	9E-11	10.0457574905607	23001564	Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans.	Telomere length	0	0	1	1
rs8001641	9E-11	10.0457574905607	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs780093	9E-11	10.0457574905607	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	0	0	0
rs12565727	9E-11	10.0457574905607	22693459	Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.	Male-pattern baldness	0	1	1	1
rs1127065	9E-11	10.0457574905607	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	0	0	0
rs2545801	9E-11	10.0457574905607	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Metabolite levels	0	0	1	1
rs7412746	9E-11	10.0457574905607	21983785	Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3.	Melanoma	0	1	1	1
rs6747972	9E-11	10.0457574905607	21779176	Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.	Restless legs syndrome	1	1	1	1
rs11249215	9E-11	10.0457574905607	21743469	Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.	Ankylosing spondylitis	1	1	1	1
rs3849942	9E-11	10.0457574905607	20801718	Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.	Amyotrophic lateral sclerosis	1	1	1	1
rs12447690	9E-11	10.0457574905607	20485516	Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.	Central corneal thickness	0	0	1	1
rs7809799	9E-11	10.0457574905607	20228798	Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL).	Ulcerative colitis	0	1	1	1
rs365990	9E-11	10.0457574905607	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	1	1	1
rs3129934	9E-11	10.0457574905607	18941528	Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms.	Multiple sclerosis	0	0	1	1
rs7216389	9E-11	10.0457574905607	17611496	Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma.	Asthma	0	1	1	1
rs17101923	1E-10	10	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (number of teeth)	0	1	0	0
rs13030174	1E-10	10	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs310405	1E-10	10	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs6450922	1E-10	10	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs887912	1E-10	10	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs2588809	1E-10	10	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	0	1	1	1
rs16997087	1E-10	10	23471985	Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.	Brain connectivity	1	1	1	1
rs17819300	1E-10	10	23471985	Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.	Brain connectivity	1	1	1	1
rs7839059	1E-10	10	23437003	Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure.	Bone mineral density	0	1	1	1
rs6857	1E-10	10	23419831	APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.	Alzheimer's disease biomarkers	0	0	0	0
rs17183295	1E-10	10	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs17348299	1E-10	10	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs12342831	1E-10	10	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2186369	1E-10	10	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs909674	1E-10	10	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11847263	1E-10	10	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11190134	1E-10	10	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs3892630	1E-10	10	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs2463822	1E-10	10	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	0	0	0
rs6585424	1E-10	10	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	0	0	0
rs1440581	1E-10	10	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	0	1	1
rs2306786	1E-10	10	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	1	1	1	1
rs6010620	1E-10	10	22886559	Genome-wide association study of glioma and meta-analysis.	Glioma	0	0	1	1
rs4609139	1E-10	10	22792070	Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus.	Bone mineral density	0	0	0	0
rs1321311	1E-10	10	22634755	Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.	Colorectal cancer	0	1	1	1
rs673548	1E-10	10	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs67418890	1E-10	10	22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Lipid metabolism phenotypes	1	1	1	1
rs4886238	1E-10	10	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs17030845	1E-10	10	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs2070729	1E-10	10	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs399604	1E-10	10	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs7961894	1E-10	10	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	0	0
rs8006385	1E-10	10	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs7756935	1E-10	10	22003152	Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies.	Lipoprotein-associated phospholipase A2 activity and mass	0	0	0	0
rs805303	1E-10	10	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Hypertension	0	1	0	0
rs17608766	1E-10	10	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	0	1	1	1
rs13107325	1E-10	10	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs2304256	1E-10	10	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	1	1	1
rs2108622	1E-10	10	21729881	Genome-wide association study identifies common variants associated with circulating vitamin E levels.	Vitamin E levels	0	1	1	1
rs15285	1E-10	10	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Triglycerides-Blood Pressure (TG-BP)	0	1	0	0
rs2895811	1E-10	10	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	1	1	1	1
rs744373	1E-10	10	21390209	Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease.	Alzheimer's disease (late onset)	0	0	1	1
rs11676348	1E-10	10	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs907611	1E-10	10	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	1	1	1	1
rs401681	1E-10	10	21160077	Genetic correction of PSA values using sequence variants associated with PSA levels.	Prostate-specific antigen levels	0	1	1	1
rs17268785	1E-10	10	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs2549794	1E-10	10	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs3764147	1E-10	10	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs11848785	1E-10	10	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs883079	1E-10	10	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	0	1	1	1
rs2890652	1E-10	10	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs7155279	1E-10	10	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs11206510	1E-10	10	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	LDL cholesterol	0	0	1	1
rs12027135	1E-10	10	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs9686661	1E-10	10	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	1	1	1	1
rs10965250	1E-10	10	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	0	0	1	1
rs499697	1E-10	10	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs2230199	1E-10	10	20385819	Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs2277027	1E-10	10	20010835	Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.	Pulmonary function	0	1	1	1
rs941576	1E-10	10	19966805	The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs855791	1E-10	10	19820699	Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.	Iron status biomarkers	0	0	1	1
rs6013509	1E-10	10	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hemoglobin	1	1	1	1
rs11239550	1E-10	10	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	0	1	1	1
rs857721	1E-10	10	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Other erythrocyte phenotypes	0	1	1	1
rs893001	1E-10	10	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	NA	NA	NA	NA
rs7193343	1E-10	10	19597491	A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.	Atrial fibrillation	0	0	1	1
rs2231142	1E-10	10	19503597	Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.	Uric acid levels	0	0	0	0
rs236114	1E-10	10	19448619	Loci at chromosomes 13, 19 and 20 influence age at natural menopause.	Menopause (age at onset)	0	0	1	1
rs1004467	1E-10	10	19430479	Genome-wide association study of blood pressure and hypertension.	Systolic blood pressure	0	0	1	1
rs8034191	1E-10	10	19300482	A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci.	Chronic obstructive pulmonary disease	0	1	1	1
rs4143832	1E-10	10	19198610	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.	Eosinophil counts	0	1	1	1
rs1800562	1E-10	10	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	0	0	0
rs2338104	1E-10	10	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	HDL cholesterol	0	0	1	1
rs10958409	1E-10	10	18997786	Susceptibility loci for intracranial aneurysm in European and Japanese populations.	Intracranial aneurysm	1	1	1	1
rs1333040	1E-10	10	18997786	Susceptibility loci for intracranial aneurysm in European and Japanese populations.	Intracranial aneurysm	0	0	1	1
rs1880887	1E-10	10	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs10778213	1E-10	10	18439548	Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.	C-reactive protein	0	0	1	1
rs11205277	1E-10	10	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs6830062	1E-10	10	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs7153027	1E-10	10	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs12779790	1E-10	10	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	0	1	1	1
rs13277113	1E-10	10	18204098	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.	Systemic lupus erythematosus	1	1	1	1
rs4149268	1E-10	10	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs2373115	1E-10	10	17553421	GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers.	Alzheimer's disease (late onset)	1	1	1	1
rs1219648	1E-10	10	17529973	A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.	Breast cancer	0	0	1	1
rs224136	1E-10	10	17435756	Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.	Crohn's disease	1	1	1	1
rs10494366	1E-10	10	16648850	A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.	QT interval	0	0	1	1
rs3744061	2E-10	9.69897000433602	23776548	Genetic loci for retinal arteriolar microcirculation.	Retinal arteriolar caliber	1	1	1	1
rs6568401	2E-10	9.69897000433602	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (time to first tooth eruption)	1	1	1	1
rs2720460	2E-10	9.69897000433602	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	1	1	1	1
rs522162	2E-10	9.69897000433602	23577725	Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.	Age-related macular degeneration	0	0	1	1
rs7466269	2E-10	9.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs1545552	2E-10	9.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs718444	2E-10	9.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs12446632	2E-10	9.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs1412239	2E-10	9.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	NA	NA	NA	NA
rs10875976	2E-10	9.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs1294421	2E-10	9.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Waist-hip ratio	0	0	1	1
rs2405942	2E-10	9.69897000433602	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	NA	NA	NA	NA
rs616488	2E-10	9.69897000433602	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs527616	2E-10	9.69897000433602	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs3760982	2E-10	9.69897000433602	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs7879933	2E-10	9.69897000433602	23471985	Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.	Brain connectivity	NA	NA	NA	NA
rs11755845 	2E-10	9.69897000433602	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	NA	NA	NA	NA
rs499368	2E-10	9.69897000433602	23378610	Genetic variants associated with glycine metabolism and their role in insulin sensitivity and type 2 diabetes.	Metabolite levels	1	1	1	1
rs909674	2E-10	9.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1122979	2E-10	9.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9268853	2E-10	9.69897000433602	23349640	Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.	Lymphoma	0	1	1	1
rs1564892	2E-10	9.69897000433602	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs10982156	2E-10	9.69897000433602	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	1	1	1	1
rs17050272	2E-10	9.69897000433602	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs4939827	2E-10	9.69897000433602	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	0	0	1	1
rs2074488	2E-10	9.69897000433602	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	1	1	1
rs4802307	2E-10	9.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs1847472	2E-10	9.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs16872571	2E-10	9.69897000433602	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs13277113	2E-10	9.69897000433602	23053960	Genome-wide pathway analysis of genome-wide association studies on systemic lupus erythematosus and rheumatoid arthritis.	Systemic lupus erythematosus	0	0	1	1
rs6486122	2E-10	9.69897000433602	22990020	Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation.	Plasminogen activator inhibitor type 1 levels (PAI-1)	1	1	1	1
rs9383938	2E-10	9.69897000433602	22976474	A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.	Breast cancer	0	0	1	1
rs7202116	2E-10	9.69897000433602	22982992	FTO genotype is associated with phenotypic variability of body mass index.	Body mass index	0	0	1	1
rs4149310	2E-10	9.69897000433602	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	1	1	1	1
rs2411984	2E-10	9.69897000433602	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	0	0	0
rs2707466	2E-10	9.69897000433602	22792071	WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk.	Cortical thickness	0	1	0	0
rs13179048	2E-10	9.69897000433602	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs4841132	2E-10	9.69897000433602	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	0	1	1	1
rs9258260	2E-10	9.69897000433602	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	0	1	1	1
rs8060686	2E-10	9.69897000433602	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs12456492	2E-10	9.69897000433602	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	1	1	1	1
rs964184	2E-10	9.69897000433602	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	0	1	1	1
rs2271893	2E-10	9.69897000433602	22182935	Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.	Bipolar disorder	1	1	1	1
rs11789898	2E-10	9.69897000433602	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs941207	2E-10	9.69897000433602	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	0	0
rs8022206	2E-10	9.69897000433602	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs11628318	2E-10	9.69897000433602	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs2297067	2E-10	9.69897000433602	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	0	0
rs6857	2E-10	9.69897000433602	22005931	Genome-wide association analysis of age-at-onset in Alzheimer's disease.	Alzheimer's disease (age of onset)	0	0	0	0
rs6984305	2E-10	9.69897000433602	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alkaline phosphatase)	0	1	1	1
rs2857595	2E-10	9.69897000433602	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	1	1	1
rs6903823	2E-10	9.69897000433602	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs508487	2E-10	9.69897000433602	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	1	1	1
rs13139571	2E-10	9.69897000433602	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	1	1	1	1
rs1799945	2E-10	9.69897000433602	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Hypertension	0	1	0	0
rs1549318	2E-10	9.69897000433602	21873549	Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.	Proinsulin levels	1	1	1	1
rs2119704	2E-10	9.69897000433602	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs10201872	2E-10	9.69897000433602	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs9891119	2E-10	9.69897000433602	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs10488631	2E-10	9.69897000433602	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	0	1	1
rs651164	2E-10	9.69897000433602	21743057	Genome-wide association study identifies new prostate cancer susceptibility loci.	Prostate cancer	NA	NA	NA	NA
rs4665058	2E-10	9.69897000433602	21738491	Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals.	Sudden cardiac arrest	1	1	1	1
rs2523822	2E-10	9.69897000433602	21570397	Susceptibility to amoxicillin-clavulanate-induced liver injury is influenced by multiple HLA class I and II alleles.	Drug-induced liver injury (amoxicillin-clavulanate)	0	1	1	1
rs538147	2E-10	9.69897000433602	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	0	1	1	1
rs943072	2E-10	9.69897000433602	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	1	1	1	1
rs2297441	2E-10	9.69897000433602	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs212388	2E-10	9.69897000433602	21298027	A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease.	Crohn's disease and celiac disease	0	1	1	1
rs13387042	2E-10	9.69897000433602	21263130	Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study.	Breast cancer	0	0	1	1
rs865686	2E-10	9.69897000433602	21263130	Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study.	Breast cancer	0	0	1	1
rs13187289	2E-10	9.69897000433602	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs4902642	2E-10	9.69897000433602	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs11169552	2E-10	9.69897000433602	20972440	Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.	Colorectal cancer	1	1	1	1
rs4925386	2E-10	9.69897000433602	20972440	Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.	Colorectal cancer	1	1	1	1
rs710521	2E-10	9.69897000433602	20972438	A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.	Bladder cancer	1	1	1	1
rs1582931	2E-10	9.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs11867479	2E-10	9.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs11754661	2E-10	9.69897000433602	20885792	Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.	Alzheimer's disease (late onset)	1	1	1	1
rs3129882	2E-10	9.69897000433602	20711177	Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.	Parkinson's disease	0	0	1	1
rs7941030	2E-10	9.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	1	1	1	1
rs9488822	2E-10	9.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	1	1	1	1
rs492602	2E-10	9.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	1	1
rs2255141	2E-10	9.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	1	1	1	1
rs4148008	2E-10	9.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs10195252	2E-10	9.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	1	1
rs17287293	2E-10	9.69897000433602	20639392	Genome-wide association analysis identifies multiple loci related to resting heart rate.	Resting heart rate	0	1	1	1
rs972283	2E-10	9.69897000433602	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	0	1	1	1
rs8042680	2E-10	9.69897000433602	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	1	1	1	1
rs1003719	2E-10	9.69897000433602	20463881	Digital quantification of human eye color highlights genetic association of three new loci.	Eye color traits	1	1	1	1
rs9657904	2E-10	9.69897000433602	20453840	Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs13387042	2E-10	9.69897000433602	20453838	Genome-wide association study identifies five new breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs12571093	2E-10	9.69897000433602	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (disc)	0	1	1	1
rs1317209	2E-10	9.69897000433602	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	1	1	1	1
rs10903122	2E-10	9.69897000433602	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs3790844	2E-10	9.69897000433602	20101243	A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33.	Pancreatic cancer	1	1	1	1
rs2736100	2E-10	9.69897000433602	19836008	A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.	Lung adenocarcinoma	0	1	1	1
rs31489	2E-10	9.69897000433602	19836008	A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.	Lung adenocarcinoma	0	1	1	1
rs2941740	2E-10	9.69897000433602	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (hip)	0	1	0	0
rs4729260	2E-10	9.69897000433602	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	0	1	0	0
rs1327301	2E-10	9.69897000433602	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	NA	NA	NA	NA
rs526934	2E-10	9.69897000433602	19744961	Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.	Folate pathway vitamin levels	1	1	1	1
rs2294008	2E-10	9.69897000433602	19648920	Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer.	Bladder cancer	0	0	1	1
rs2880058	2E-10	9.69897000433602	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	QT interval	0	0	1	1
rs1412829	2E-10	9.69897000433602	19578366	Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.	Glioma (high-grade)	0	1	1	1
rs3131296	2E-10	9.69897000433602	19571808	Common variants conferring risk of schizophrenia.	Schizophrenia	0	1	1	1
rs6495122	2E-10	9.69897000433602	19430479	Genome-wide association study of blood pressure and hypertension.	Diastolic blood pressure	0	0	1	1
rs4307059	2E-10	9.69897000433602	19404256	Common genetic variants on 5p14.1 associate with autism spectrum disorders.	Autism	1	1	1	1
rs2981579	2E-10	9.69897000433602	19330030	A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).	Breast cancer	0	0	1	1
rs2562456	2E-10	9.69897000433602	19207018	Genome-wide association study of acute post-surgical pain in humans.	Pain	1	1	1	1
rs6929137	2E-10	9.69897000433602	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (spine)	0	0	1	1
rs174570	2E-10	9.69897000433602	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	0	0	0
rs1532085	2E-10	9.69897000433602	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	HDL cholesterol	0	0	1	1
rs961253	2E-10	9.69897000433602	19011631	Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer.	Colorectal cancer	1	1	1	1
rs1169313	2E-10	9.69897000433602	18940312	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.	Liver enzyme levels	0	1	1	1
rs2200733	2E-10	9.69897000433602	18991354	Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke.	Stroke (ischemic)	0	0	1	1
rs17483466	2E-10	9.69897000433602	18758461	A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia.	Chronic lymphocytic leukemia	1	1	1	1
rs7746082	2E-10	9.69897000433602	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	1	1	1
rs1748195	2E-10	9.69897000433602	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs13361189	2E-10	9.69897000433602	17554261	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.	Crohn's disease	0	0	1	1
rs7903146	2E-10	9.69897000433602	17460697	A variant in CDKAL1 influences insulin response and risk of type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs870142	3E-10	9.52287874528034	23708191	Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.	Congenital heart disease	1	1	1	1
rs6662509	3E-10	9.52287874528034	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs2844479	3E-10	9.52287874528034	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	1	1	1
rs153750	3E-10	9.52287874528034	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs1957894	3E-10	9.52287874528034	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	1	1	1	1
rs7141529	3E-10	9.52287874528034	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs2072590	3E-10	9.52287874528034	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	0	0	0	0
rs9303542	3E-10	9.52287874528034	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	1	1	1	1
rs1805007	3E-10	9.52287874528034	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Non-melanoma skin cancer	0	1	0	0
rs12966547	3E-10	9.52287874528034	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs17776563	3E-10	9.52287874528034	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs4804416	3E-10	9.52287874528034	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	1	1	1
rs1261117	3E-10	9.52287874528034	23894747	A comprehensive family-based replication study of schizophrenia genes.	Schizophrenia	1	1	1	1
rs12342831	3E-10	9.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs17348299	3E-10	9.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4718428	3E-10	9.52287874528034	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs3916164	3E-10	9.52287874528034	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs11072566	3E-10	9.52287874528034	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs907611	3E-10	9.52287874528034	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs2231884	3E-10	9.52287874528034	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs194749	3E-10	9.52287874528034	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs13172324	3E-10	9.52287874528034	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	NA	NA	NA	NA
rs9936833	3E-10	9.52287874528034	22961001	Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.	Barrett's esophagus	1	1	1	1
rs2076756	3E-10	9.52287874528034	22936669	A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.	Crohn's disease	0	0	1	1
rs10211524	3E-10	9.52287874528034	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	0	1	1
rs16850360	3E-10	9.52287874528034	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	1	1	1	1
rs8001641	3E-10	9.52287874528034	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	0	0	0	0
rs3132306	3E-10	9.52287874528034	22814818	Population-based meta-analysis in Caucasians confirms association with COL5A1 and ZNF469 but not COL8A2 with central corneal thickness.	Central corneal thickness	0	1	1	1
rs4958881	3E-10	9.52287874528034	23055271	Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.	Myasthenia gravis 	1	1	1	1
rs6573333	3E-10	9.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs11708067	3E-10	9.52287874528034	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs780094	3E-10	9.52287874528034	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	0	1	0	0
rs10028213	3E-10	9.52287874528034	22494929	Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function.	Thyroid function	0	1	1	1
rs1042725	3E-10	9.52287874528034	22504419	Common variants at 12q15 and 12q24 are associated with infant head circumference.	Head circumference (infant)	0	1	1	1
rs6488898	3E-10	9.52287874528034	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	1	1	1	1
rs7618915	3E-10	9.52287874528034	22182935	Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.	Bipolar disorder	0	1	1	1
rs11199874	3E-10	9.52287874528034	22130093	New variants at 10q26 and 15q21 are associated with aggressive prostate cancer in a genome-wide association study from a prostate biopsy screening cohort.	Prostate cancer	0	1	1	1
rs4246215	3E-10	9.52287874528034	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs8109288	3E-10	9.52287874528034	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	0	0
rs4074793	3E-10	9.52287874528034	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs1173771	3E-10	9.52287874528034	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Hypertension	0	1	0	0
rs11581062	3E-10	9.52287874528034	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs1975197	3E-10	9.52287874528034	21779176	Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.	Restless legs syndrome	1	1	1	1
rs2116830	3E-10	9.52287874528034	21708048	Genome wide association study identifies KCNMA1 contributing to human obesity.	Obesity	1	1	1	1
rs10513789	3E-10	9.52287874528034	21738487	Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.	Parkinson's disease	0	0	1	1
rs12189362	3E-10	9.52287874528034	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs780093	3E-10	9.52287874528034	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Triglycerides-Blood Pressure (TG-BP)	0	1	0	0
rs1746048	3E-10	9.52287874528034	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	1	1	1	1
rs599839	3E-10	9.52287874528034	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	1	1	1
rs12989701	3E-10	9.52287874528034	21390209	Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease.	Alzheimer's disease (late onset)	0	0	0	0
rs2298428	3E-10	9.52287874528034	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	0	1	1	1
rs10850409	3E-10	9.52287874528034	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	0	1	1	1
rs17391905	3E-10	9.52287874528034	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs4112788	3E-10	9.52287874528034	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	1	1	1	1
rs1043515	3E-10	9.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs4821083	3E-10	9.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	NA	NA	NA	NA
rs10152591	3E-10	9.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs442177	3E-10	9.52287874528034	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs12328675	3E-10	9.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	0	0
rs4765127	3E-10	9.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs1689800	3E-10	9.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs10488631	3E-10	9.52287874528034	20639880	Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis.	Primary biliary cirrhosis	0	0	1	1
rs5945326	3E-10	9.52287874528034	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	NA	NA	NA	NA
rs12931267	3E-10	9.52287874528034	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Hair color	0	0	0	0
rs3858145	3E-10	9.52287874528034	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (disc)	0	0	0	0
rs8068318	3E-10	9.52287874528034	20383145	Genetic loci influencing kidney function and chronic kidney disease.	Creatinine levels	0	1	1	1
rs1893217	3E-10	9.52287874528034	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs744166	3E-10	9.52287874528034	20159113	Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.	Multiple sclerosis	0	0	1	1
rs1260326	3E-10	9.52287874528034	20081857	Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.	Two-hour glucose challenge	0	1	1	1
rs1321311	3E-10	9.52287874528034	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	1	1	1
rs10889353	3E-10	9.52287874528034	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs11209026	3E-10	9.52287874528034	19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Ulcerative colitis	0	0	1	1
rs4820268	3E-10	9.52287874528034	19853236	Sequence variants in three loci influence monocyte counts and erythrocyte volume.	Hematology traits	0	0	0	0
rs1122794	3E-10	9.52287874528034	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular hemoglobin	0	1	0	0
rs7524102	3E-10	9.52287874528034	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	0	1	1	1
rs10934853	3E-10	9.52287874528034	19767754	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.	Prostate cancer	1	1	1	1
rs2108622	3E-10	9.52287874528034	19578179	A genome-wide association study of acenocoumarol maintenance dosage.	Acenocoumarol maintenance dosage	0	1	1	1
rs2300747	3E-10	9.52287874528034	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs35391	3E-10	9.52287874528034	19340012	Genome-wide association study of tanning phenotype in a population of European ancestry.	Tanning	0	1	1	1
rs6586282	3E-10	9.52287874528034	20031578	Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study.	Homocysteine levels	1	1	1	1
rs2108622	3E-10	9.52287874528034	19300499	A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose.	Warfarin maintenance dose	0	1	1	1
rs7498665	3E-10	9.52287874528034	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Body mass index	0	0	1	1
rs6756629	3E-10	9.52287874528034	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	LDL cholesterol	0	1	0	0
rs471364	3E-10	9.52287874528034	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	HDL cholesterol	0	0	1	1
rs10492972	3E-10	9.52287874528034	18997785	Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs281437	3E-10	9.52287874528034	18604267	Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women.	Soluble ICAM-1	0	0	0	0
rs11175593	3E-10	9.52287874528034	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs4263839	3E-10	9.52287874528034	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs4963128	3E-10	9.52287874528034	18204446	Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.	Systemic lupus erythematosus	1	1	1	1
rs3890182	3E-10	9.52287874528034	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	HDL cholesterol	0	0	1	1
rs1859962	3E-10	9.52287874528034	17603485	Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes.	Prostate cancer	0	0	1	1
rs9320913	4E-10	9.39794000867204	23722424	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.	Educational attainment	1	1	1	1
rs838145	4E-10	9.39794000867204	23636237	Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake.	Dietary macronutrient intake	0	1	1	1
rs11578508	4E-10	9.39794000867204	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs2982712	4E-10	9.39794000867204	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs4735692	4E-10	9.39794000867204	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs941764	4E-10	9.39794000867204	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs1336472:rs4715555	4E-10	9.39794000867204	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs7829127	4E-10	9.39794000867204	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs657152	4E-10	9.39794000867204	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	1	1	1
rs2647045	4E-10	9.39794000867204	23349640	Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.	Lymphoma	0	0	0	0
rs9266629	4E-10	9.39794000867204	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	1	1	1
rs9491697	4E-10	9.39794000867204	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	0	1	1	1
rs4836519	4E-10	9.39794000867204	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs12722515	4E-10	9.39794000867204	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs7739264	4E-10	9.39794000867204	23104006	Genome-wide association meta-analysis identifies new endometriosis risk loci.	Endometriosis	1	1	1	1
rs3824999	4E-10	9.39794000867204	22634755	Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.	Colorectal cancer	1	1	1	1
rs59374417	4E-10	9.39794000867204	22561518	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.	Vitiligo	1	1	1	1
rs4948418	4E-10	9.39794000867204	22182935	Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.	Bipolar disorder	1	1	1	1
rs3809566	4E-10	9.39794000867204	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs17356664	4E-10	9.39794000867204	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs4373814	4E-10	9.39794000867204	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	0	1	0	0
rs1016343	4E-10	9.39794000867204	21743057	Genome-wide association study identifies new prostate cancer susceptibility loci.	Prostate cancer	1	1	1	1
rs10033900	4E-10	9.39794000867204	21665990	Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs3813579	4E-10	9.39794000867204	21565293	Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.	Thyroid volume	0	0	0	0
rs9272105	4E-10	9.39794000867204	21502966	Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients.	Response to interferon beta therapy	0	1	1	1
rs12936587	4E-10	9.39794000867204	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	1	1	1	1
rs9982601	4E-10	9.39794000867204	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	1	1	1
rs7574865	4E-10	9.39794000867204	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	0	1	1	1
rs2102808	4E-10	9.39794000867204	21292315	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.	Parkinson's disease	1	1	1	1
rs3112612	4E-10	9.39794000867204	21263130	Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study.	Breast cancer	0	0	1	1
rs7642134	4E-10	9.39794000867204	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs6784615	4E-10	9.39794000867204	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	1	1	1	1
rs1555543	4E-10	9.39794000867204	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs13088462	4E-10	9.39794000867204	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs7926971	4E-10	9.39794000867204	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2277862	4E-10	9.39794000867204	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	1	1
rs4660293	4E-10	9.39794000867204	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	1	1
rs11613352	4E-10	9.39794000867204	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	1	1
rs4293393	4E-10	9.39794000867204	20686651	Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases.	Chronic kidney disease and serum creatinine levels	0	1	1	1
rs281868	4E-10	9.39794000867204	20639392	Genome-wide association analysis identifies multiple loci related to resting heart rate.	Resting heart rate	0	1	1	1
rs2153271	4E-10	9.39794000867204	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Freckling	0	1	1	1
rs951005	4E-10	9.39794000867204	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	1	1	1	1
rs3813948	4E-10	9.39794000867204	20212171	C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies.	C4b binding protein levels	1	1	1	1
rs10806425	4E-10	9.39794000867204	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs673548	4E-10	9.39794000867204	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs4939883	4E-10	9.39794000867204	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs10500264	4E-10	9.39794000867204	19915574	Common variants at five new loci associated with early-onset inflammatory bowel disease.	Inflammatory bowel disease (early onset)	0	1	1	1
rs7385804	4E-10	9.39794000867204	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hematocrit	0	1	0	0
rs9374080	4E-10	9.39794000867204	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	0	1	1	1
rs9609565	4E-10	9.39794000867204	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Hematological parameters	0	1	1	1
rs3117582	4E-10	9.39794000867204	19654303	Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.	Lung cancer	0	1	1	1
rs3118914	4E-10	9.39794000867204	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs1038304	4E-10	9.39794000867204	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (hip)	0	0	0	0
rs1260326	4E-10	9.39794000867204	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	Metabolic traits	0	0	1	1
rs5743289	4E-10	9.39794000867204	18758464	Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs7770628	4E-10	9.39794000867204	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	1	1	1
rs10516487	4E-10	9.39794000867204	18204447	Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus.	Systemic lupus erythematosus	0	1	1	1
rs10883365	4E-10	9.39794000867204	17554261	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.	Crohn's disease	0	0	1	1
rs1175550	5E-10	9.30102999566398	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Cu levels)	1	1	1	1
rs6957923	5E-10	9.30102999566398	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs3850699	5E-10	9.30102999566398	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs380904:rs8086028	5E-10	9.30102999566398	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs909674	5E-10	9.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10813951	5E-10	9.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2186369	5E-10	9.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs12913547	5E-10	9.30102999566398	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	0	1	1	1
rs3811444	5E-10	9.30102999566398	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs560426	5E-10	9.30102999566398	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	0	0	0	0
rs17625845	5E-10	9.30102999566398	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs12373124	5E-10	9.30102999566398	22693459	Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.	Male-pattern baldness	0	1	1	1
rs908327	5E-10	9.30102999566398	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	NA	NA	NA	NA
rs2293941	5E-10	9.30102999566398	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	1	1	1	1
rs2835872	5E-10	9.30102999566398	22554406	Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6.	Electroencephalographic traits in alcoholism	1	1	1	1
rs1027643	5E-10	9.30102999566398	22544364	A genome-wide association study identifies susceptibility loci for Wilms tumor.	Wilms tumor	1	1	1	1
rs7259004	5E-10	9.30102999566398	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Sphingolipid levels	1	1	1	1
rs10512627	5E-10	9.30102999566398	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs6995402	5E-10	9.30102999566398	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs1466535	5E-10	9.30102999566398	22055160	Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1.	Abdominal aortic aneurysm	1	1	1	1
rs2425752	5E-10	9.30102999566398	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs3024505	5E-10	9.30102999566398	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	1	1	1
rs6710518	5E-10	9.30102999566398	21533022	Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.	Bone mineral density	1	1	1	1
rs6701713	5E-10	9.30102999566398	21460841	Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.	Alzheimer's disease (late onset)	0	1	1	1
rs3811647	5E-10	9.30102999566398	21483845	Genome-wide association study identifies genetic loci associated with iron deficiency.	Iron status biomarkers	0	0	1	1
rs4234798	5E-10	9.30102999566398	21216879	A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3.	Insulin-like growth factors	1	1	1	1
rs2062305	5E-10	9.30102999566398	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs7342028	5E-10	9.30102999566398	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs17608766	5E-10	9.30102999566398	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	0	1	1	1
rs3099844	5E-10	9.30102999566398	20662065	Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus.	Neonatal lupus	0	1	1	1
rs7025486	5E-10	9.30102999566398	20622881	Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.	Abdominal aortic aneurysm	1	1	1	1
rs2721051	5E-10	9.30102999566398	20485516	Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.	Central corneal thickness	0	1	1	1
rs934734	5E-10	9.30102999566398	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	1	1	1	1
rs11129795	5E-10	9.30102999566398	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	1	1	1
rs7385804	5E-10	9.30102999566398	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Hematological parameters	0	1	1	1
rs445114	5E-10	9.30102999566398	19767754	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.	Prostate cancer	0	1	1	1
rs10517086	5E-10	9.30102999566398	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs12619285	5E-10	9.30102999566398	19198610	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.	Eosinophil counts	1	1	1	1
rs1402837	5E-10	9.30102999566398	19096518	Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study.	Glycated hemoglobin levels	0	0	1	1
rs6265	5E-10	9.30102999566398	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Body mass index	0	0	1	1
rs10903129	5E-10	9.30102999566398	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	0	1	1
rs3117582	5E-10	9.30102999566398	18978787	Common 5p15.33 and 6p21.33 variants influence lung cancer risk.	Lung cancer	0	0	1	1
rs12355784	5E-10	9.30102999566398	18940312	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.	Liver enzyme levels	0	1	1	1
rs7240405	5E-10	9.30102999566398	20031538	Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions.	HDL cholesterol	0	0	1	1
rs2076756	5E-10	9.30102999566398	17068223	A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.	Inflammatory bowel disease	0	0	1	1
rs2030323	6E-10	9.22184874961636	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Body mass index	0	0	0	0
rs2618516	6E-10	9.22184874961636	23471985	Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.	Brain connectivity	1	1	1	1
rs3817963	6E-10	9.22184874961636	23472185	Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.	Multiple sclerosis (OCB status)	0	0	0	0
rs17648524	6E-10	9.22184874961636	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs10519227	6E-10	9.22184874961636	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs1122979	6E-10	9.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs909674	6E-10	9.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7090871	6E-10	9.22184874961636	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs7702331	6E-10	9.22184874961636	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	0	0	1	1
rs6142618	6E-10	9.22184874961636	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs11150589	6E-10	9.22184874961636	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	1	1	1	1
rs7078160	6E-10	9.22184874961636	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	0	0	0	0
rs17252936	6E-10	9.22184874961636	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	NA	NA	NA	NA
rs11171846	6E-10	9.22184874961636	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs3813582	6E-10	9.22184874961636	22494929	Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function.	Thyroid function	0	1	1	1
rs1883025	6E-10	9.22184874961636	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs754466	6E-10	9.22184874961636	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs17249754	6E-10	9.22184874961636	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	0	0	0
rs12466022	6E-10	9.22184874961636	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs3130573	6E-10	9.22184874961636	21750679	Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.	Systemic sclerosis	0	1	1	1
rs11767557	6E-10	9.22184874961636	21460841	Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.	Alzheimer's disease (late onset)	1	1	1	1
rs1800562	6E-10	9.22184874961636	21483845	Genome-wide association study identifies genetic loci associated with iron deficiency.	Iron status biomarkers	0	0	1	1
rs266849	6E-10	9.22184874961636	21160077	Genetic correction of PSA values using sequence variants associated with PSA levels.	Prostate-specific antigen levels	0	0	0	0
rs694739	6E-10	9.22184874961636	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs991014	6E-10	9.22184874961636	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs7332115	6E-10	9.22184874961636	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	0	1	1
rs7916441	6E-10	9.22184874961636	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1800562	6E-10	9.22184874961636	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	1	1
rs314370	6E-10	9.22184874961636	20639392	Genome-wide association analysis identifies multiple loci related to resting heart rate.	Resting heart rate	0	1	1	1
rs2900333	6E-10	9.22184874961636	20543847	Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer.	Testicular germ cell cancer	0	1	1	1
rs1329650	6E-10	9.22184874961636	20418890	Genome-wide meta-analyses identify multiple loci associated with smoking behavior.	Smoking behavior	1	1	1	1
rs7117858	6E-10	9.22184874961636	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (hip)	1	1	1	1
rs12085006	6E-10	9.22184874961636	19744961	Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.	Folate pathway vitamin levels	0	1	1	1
rs511154	6E-10	9.22184874961636	20031576	Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts.	Fibrinogen	1	1	1	1
rs560887	6E-10	9.22184874961636	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	Metabolic traits	0	1	1	1
rs13397985	6E-10	9.22184874961636	18758461	A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia.	Chronic lymphocytic leukemia	0	1	1	1
rs4626664	6E-10	9.22184874961636	18660810	PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome.	Restless legs syndrome	1	1	1	1
rs10946808	6E-10	9.22184874961636	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs8007661	6E-10	9.22184874961636	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	0	0	1	1
rs11107116	6E-10	9.22184874961636	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs3802842	6E-10	9.22184874961636	18372901	Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.	Colorectal cancer	1	1	1	1
rs9364554	6E-10	9.22184874961636	18264097	Multiple newly identified loci associated with prostate cancer susceptibility.	Prostate cancer	0	1	1	1
rs1111875	6E-10	9.22184874961636	17463246	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	Type 2 diabetes	0	0	1	1
rs1111875	6E-10	9.22184874961636	17463248	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.	Type 2 diabetes	0	0	1	1
rs4965593	7E-10	9.15490195998574	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs11782652	7E-10	9.15490195998574	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	1	1	1	1
rs6815916:rs6092326	7E-10	9.15490195998574	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs2217560	7E-10	9.15490195998574	23502781	Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension.	Pulmonary arterial hypertension (without BMPR2 mutations)	1	1	1	1
rs6583437	7E-10	9.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs12940030	7E-10	9.15490195998574	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs2227564	7E-10	9.15490195998574	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs10896794	7E-10	9.15490195998574	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs7766070	7E-10	9.15490195998574	22693455	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.	Type 2 diabetes	0	0	0	0
rs5934683	7E-10	9.15490195998574	22634755	Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.	Colorectal cancer	NA	NA	NA	NA
rs4822024	7E-10	9.15490195998574	22561518	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.	Vitiligo	1	1	1	1
rs7267979	7E-10	9.15490195998574	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alkaline phosphatase)	1	1	1	1
rs633185	7E-10	9.15490195998574	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs2982694	7E-10	9.15490195998574	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs4430796	7E-10	9.15490195998574	21499250	Genome-wide association study identifies a common variant associated with risk of endometrial cancer.	Endometrial cancer	0	1	1	1
rs12261843	7E-10	9.15490195998574	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs2597513	7E-10	9.15490195998574	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs751543	7E-10	9.15490195998574	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs3792752	7E-10	9.15490195998574	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	0	0	0
rs1990760	7E-10	9.15490195998574	20694011	Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.	Immunoglobulin A 	0	1	1	1
rs12670798	7E-10	9.15490195998574	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	1	1	1	1
rs12670798	7E-10	9.15490195998574	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs3127573	7E-10	9.15490195998574	20383145	Genetic loci influencing kidney function and chronic kidney disease.	Creatinine levels	0	1	1	1
rs10889353	7E-10	9.15490195998574	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs11249433	7E-10	9.15490195998574	19330030	A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).	Breast cancer	0	0	1	1
rs10761779	7E-10	9.15490195998574	18940312	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.	Liver enzyme levels	0	0	0	0
rs4624820	8E-10	9.09691001300805	23666239	Meta-analysis identifies four new loci associated with testicular germ cell tumor.	Testicular germ cell tumor	0	0	1	1
rs757210	8E-10	9.09691001300805	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	0	1	1	1
rs17536527	8E-10	9.09691001300805	23535967	Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate.	Glomerular filtration rate	0	1	1	1
rs2282015:rs13050454	8E-10	9.09691001300805	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs133885	8E-10	9.09691001300805	23423138	A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.	Mathematical ability in children with dyslexia	1	1	1	1
rs7193778	8E-10	9.09691001300805	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs2032314	8E-10	9.09691001300805	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs2476601	8E-10	9.09691001300805	23055271	Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.	Myasthenia gravis 	0	1	1	1
rs9349379	8E-10	9.09691001300805	22745674	Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis.	Coronary heart disease	0	0	0	0
rs4915077	8E-10	9.09691001300805	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	1	1	1	1
rs1061808	8E-10	9.09691001300805	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	0	1	1	1
rs1635501	8E-10	9.09691001300805	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs516246	8E-10	9.09691001300805	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	0	1	0	0
rs8124695	8E-10	9.09691001300805	21732829	Wnt signaling and Dupuytren's disease.	Dupuytren's disease	1	1	1	1
rs6812193	8E-10	9.09691001300805	21738487	Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.	Parkinson's disease	0	1	1	1
rs16942421	8E-10	9.09691001300805	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs4294134	8E-10	9.09691001300805	21623375	Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.	Paget's disease	1	1	1	1
rs1366594	8E-10	9.09691001300805	21533022	Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.	Bone mineral density	0	1	1	1
rs2341459	8E-10	9.09691001300805	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2456449	8E-10	9.09691001300805	20062064	Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk.	Chronic lymphocytic leukemia	0	1	1	1
rs87938	8E-10	9.09691001300805	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (hip)	1	1	1	1
rs7927894	8E-10	9.09691001300805	19349984	A common variant on chromosome 11q13 is associated with atopic dermatitis.	Atopic dermatitis	0	1	1	1
rs12272004	8E-10	9.09691001300805	19185284	Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study.	Carotenoid and tocopherol levels	0	1	1	1
rs1800961	8E-10	9.09691001300805	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	HDL cholesterol	0	0	1	1
rs4444235	8E-10	9.09691001300805	19011631	Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer.	Colorectal cancer	0	1	1	1
rs4355801	8E-10	9.09691001300805	18455228	Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.	Bone mineral density	0	0	1	1
rs526896	9E-10	9.04575749056067	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs7745274	9E-10	9.04575749056067	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Waist-hip ratio	0	0	1	1
rs4747011	9E-10	9.04575749056067	23471985	Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.	Brain connectivity	1	1	1	1
rs2186369	9E-10	9.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4930561	9E-10	9.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs5754217	9E-10	9.04575749056067	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs72829446	9E-10	9.04575749056067	22936694	Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men.	Androgen levels	0	0	0	0
rs12044963	9E-10	9.04575749056067	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs284489	9E-10	9.04575749056067	22570617	Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.	Glaucoma (primary open-angle)	1	1	1	1
rs12461110	9E-10	9.04575749056067	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs1260326	9E-10	9.04575749056067	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs3819299	9E-10	9.04575749056067	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs718314	9E-10	9.04575749056067	22010048	A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23.	Renal cell carcinoma	0	1	1	1
rs12968116	9E-10	9.04575749056067	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs13016963	9E-10	9.04575749056067	21983787	Genome-wide association study identifies three new melanoma susceptibility loci.	Melanoma	1	1	1	1
rs755383	9E-10	9.04575749056067	21551455	A second independent locus within DMRT1 is associated with testicular germ cell tumor susceptibility.	Testicular cancer	0	0	0	0
rs1231206	9E-10	9.04575749056067	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	1	1	1
rs3760776	9E-10	9.04575749056067	21203500	Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation.	N-glycan levels	0	0	0	0
rs17342717	9E-10	9.04575749056067	21149283	Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.	Iron status biomarkers	0	0	1	1
rs13428812	9E-10	9.04575749056067	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	1	1	1	1
rs10782001	9E-10	9.04575749056067	20953189	Genome-wide association analysis identifies three psoriasis susceptibility loci.	Psoriasis	0	1	1	1
rs4771122	9E-10	9.04575749056067	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs7112925	9E-10	9.04575749056067	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs4470914	9E-10	9.04575749056067	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1342326	9E-10	9.04575749056067	20860503	A large-scale, consortium-based genomewide association study of asthma.	Asthma	1	1	1	1
rs11136341	9E-10	9.04575749056067	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs1250552	9E-10	9.04575749056067	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs11136000	9E-10	9.04575749056067	19734902	Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.	Alzheimer's disease	1	1	1	1
rs925946	9E-10	9.04575749056067	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Body mass index	0	0	0	0
rs1635852	9E-10	9.04575749056067	18952825	Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis.	Height	0	0	1	1
rs6908425	9E-10	9.04575749056067	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	1	1	1	1
rs1701704	9E-10	9.04575749056067	18198356	A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study.	Type 1 diabetes	0	0	1	1
rs10934011	1E-9	9	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (parent-of-origin)	1	1	1	1
rs2839186	1E-9	9	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	1	1	1	1
rs1421085	1E-9	9	23636237	Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake.	Dietary macronutrient intake	0	1	1	1
rs9647379	1E-9	9	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs9596219	1E-9	9	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs10993994	1E-9	9	23555189	Genome-wide association study identifies genetic determinants of urine PCA3 levels in men.	PCA3 expression level	0	1	1	1
rs11820646	1E-9	9	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs117964204	1E-9	9	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs7648704:rs4868644	1E-9	9	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs1985317:rs827637	1E-9	9	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs2321744:rs6497540	1E-9	9	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs315122:rs884483	1E-9	9	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs6599175	1E-9	9	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (hyperdiploidy)	1	1	1	1
rs4487645	1E-9	9	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (hyperdiploidy)	0	1	1	1
rs2224003	1E-9	9	23471985	Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.	Brain connectivity	1	1	1	1
rs6909279	1E-9	9	23437003	Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure.	Bone mineral density	0	1	1	1
rs10813951	1E-9	9	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1122979	1E-9	9	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6583437	1E-9	9	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs780093 	1E-9	9	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	NA	NA	NA	NA
rs7574070	1E-9	9	23291587	Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.	Behcet's disease	1	1	1	1
rs2617170	1E-9	9	23291587	Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.	Behcet's disease	1	1	1	1
rs7606754	1E-9	9	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs1410996	1E-9	9	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	0	0	0
rs7445832	1E-9	9	23216389	Genome-wide significant association signals in IPO11-HTR1A region specific for alcohol and nicotine codependence.	Alcohol and nictotine co-dependence	1	1	1	1
rs11627546	1E-9	9	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	0	1	1	1
rs17157266	1E-9	9	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	0	0	0
rs10865331	1E-9	9	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	0	1	1	1
rs7404095	1E-9	9	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs10521318	1E-9	9	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs7240004	1E-9	9	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs4911259	1E-9	9	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs10747502	1E-9	9	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs12032643	1E-9	9	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs13408661	1E-9	9	23028483	Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA.	Asthma	0	1	1	1
rs4561508	1E-9	9	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum total protein level	0	0	0	0
rs10127775	1E-9	9	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	1	1	1
rs4374383	1E-9	9	22841784	Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.	Hepatitis C induced liver fibrosis	1	1	1	1
rs12153855	1E-9	9	22694956	Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.	Age-related macular degeneration	0	0	0	0
rs7640543	1E-9	9	22683712	Genome-wide association analysis identifies susceptibility loci for migraine without aura.	Migraine	1	1	1	1
rs10998624	1E-9	9	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-1beta)	1	1	1	1
rs6703865	1E-9	9	22745009	Multiple loci influencing hippocampal degeneration identified by genome scan.	Hippocampal atrophy	1	1	1	1
rs35747	1E-9	9	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	1	1	1	1
rs9292777	1E-9	9	22570697	Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1.	Multiple sclerosis	0	1	1	1
rs5955543	1E-9	9	22544364	A genome-wide association study identifies susceptibility loci for Wilms tumor.	Wilms tumor	NA	NA	NA	NA
rs2980879	1E-9	9	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	1	1	1
rs10838681	1E-9	9	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs10455872	1E-9	9	22368281	Genome-wide association study of genetic determinants of LDL-c response to atorvastatin therapy: importance of Lp(a).	Response to statin therapy	0	1	1	1
rs12051548	1E-9	9	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Sphingolipid levels	0	1	1	1
rs3869109	1E-9	9	22319020	A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.	Coronary heart disease	0	1	1	1
rs966423	1E-9	9	22267200	Discovery of common variants associated with low TSH levels and thyroid cancer risk.	Thyroid cancer	0	1	1	1
rs4812048	1E-9	9	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs17568628	1E-9	9	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	0	0
rs700585	1E-9	9	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs10819937	1E-9	9	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alkaline phosphatase)	1	1	1	1
rs2140773	1E-9	9	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs6888304	1E-9	9	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs8038465	1E-9	9	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs9913711	1E-9	9	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	0	1	1	1
rs4954218	1E-9	9	21979947	A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.	Corneal structure	1	1	1	1
rs2932538	1E-9	9	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	1	1	1	1
rs2932538	1E-9	9	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	0	1	0	0
rs11129295	1E-9	9	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs763361	1E-9	9	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	1	1	1
rs10488631	1E-9	9	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	0	0	0
rs12210050	1E-9	9	21700618	Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma.	Basal cell carcinoma 	0	1	1	1
rs1799899	1E-9	9	21665994	Genome-wide association study identifies two loci strongly affecting transferrin glycosylation.	Alcohol consumption (transferrin glycosylation)	0	0	0	0
rs12793173	1E-9	9	21602797	Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.	Cystic fibrosis severity	1	1	1	1
rs965469	1E-9	9	21703177	Genome-wide association study of interferon-related cytopenia in chronic hepatitis C patients.	IFN-related cytopenia	0	1	1	1
rs1545843	1E-9	9	21521612	The neuronal transporter gene SLC6A15 confers risk to major depression.	Major depressive disorder	1	1	1	1
rs10927875	1E-9	9	21459883	A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.	Dilated cardiomyopathy	1	1	1	1
rs968451	1E-9	9	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	0	1	1	1
rs3749147	1E-9	9	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Waist Circumference - Triglycerides (WC-TG)	0	0	0	0
rs12413409	1E-9	9	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	1	1	1
rs216172	1E-9	9	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	0	0	0
rs6725887	1E-9	9	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	1	1	1	1
rs12526453	1E-9	9	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	0	1	1
rs1122608	1E-9	9	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	1	1	1
rs254560	1E-9	9	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	1	1	1	1
rs10995190	1E-9	9	21278746	Common variants in ZNF365 are associated with both mammographic density and breast cancer risk.	Mammographic density	0	1	1	1
rs4939490	1E-9	9	21244703	Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data.	Multiple sclerosis	0	0	1	1
rs12700667	1E-9	9	21151130	Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis.	Endometriosis	0	1	1	1
rs17188434	1E-9	9	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs2002675	1E-9	9	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs12242110	1E-9	9	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs7784776	1E-9	9	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs6691170	1E-9	9	20972440	Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.	Colorectal cancer	1	1	1	1
rs675209	1E-9	9	20884846	Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.	Urate levels	0	0	1	1
rs1468758	1E-9	9	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1325598	1E-9	9	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1257763	1E-9	9	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs10958476	1E-9	9	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	0	0	0
rs17145738	1E-9	9	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	0	0
rs13238203	1E-9	9	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	1	1	1	1
rs3115573	1E-9	9	20595679	HLA has strongest association with IgA nephropathy in genome-wide analysis.	Nephropathy	0	1	1	1
rs896854	1E-9	9	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	1	1	1	1
rs11203203	1E-9	9	20410501	Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.	Vitiligo	1	1	1	1
rs10774021	1E-9	9	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs12413409	1E-9	9	20364137	Genome-wide association study of intracranial aneurysm identifies three new risk loci.	Intracranial aneurysm	0	1	1	1
rs1812175	1E-9	9	20397748	Genome-wide association study of height and body mass index in Australian twin families.	Height	0	0	1	1
rs4957048	1E-9	9	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	1	1	1	1
rs3817928	1E-9	9	20010835	Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.	Pulmonary function	0	1	1	1
rs4939883	1E-9	9	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs6982636	1E-9	9	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs9399137	1E-9	9	19853236	Sequence variants in three loci influence monocyte counts and erythrocyte volume.	Hematology traits	0	1	1	1
rs2075671	1E-9	9	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Other erythrocyte phenotypes	0	0	0	0
rs5756506	1E-9	9	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Hematological parameters	0	1	1	1
rs1524058	1E-9	9	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	1	1	1	1
rs3851179	1E-9	9	19734902	Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.	Alzheimer's disease	0	1	1	1
rs89107	1E-9	9	19584346	Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.	Cardiac structure and function	0	1	1	1
rs780094	1E-9	9	19503597	Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.	Uric acid levels	0	1	1	1
rs7221109	1E-9	9	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs2681472	1E-9	9	19430479	Genome-wide association study of blood pressure and hypertension.	Diastolic blood pressure	0	1	0	0
rs1530440	1E-9	9	19430483	Genome-wide association study identifies eight loci associated with blood pressure.	Diastolic blood pressure	0	1	1	1
rs12425791	1E-9	9	19369658	Genomewide association studies of stroke.	Stroke	1	1	1	1
rs3803662	1E-9	9	19330030	A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).	Breast cancer	0	0	1	1
rs17465637	1E-9	9	19198609	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.	Myocardial infarction (early onset)	1	1	1	1
rs12526453	1E-9	9	19198609	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.	Myocardial infarction (early onset)	0	1	1	1
rs9652490	1E-9	9	19182806	Variant in the sequence of the LINGO1 gene confers risk of essential tremor.	Essential tremor	1	1	1	1
rs13129697	1E-9	9	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	0	1	1	1
rs2066808	1E-9	9	19169254	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.	Psoriasis	0	1	1	1
rs1830084	1E-9	9	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	0	0	0
rs7498665	1E-9	9	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	1	0	0
rs1883025	1E-9	9	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	HDL cholesterol	0	0	1	1
rs5219	1E-9	9	19056611	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data.	Type 2 diabetes	0	0	1	1
rs6457617	1E-9	9	18668548	Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility.	Rheumatoid arthritis	0	0	1	1
rs2274910	1E-9	9	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	1	1	1	1
rs7927894	1E-9	9	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs762421	1E-9	9	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs7961581	1E-9	9	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	1	1	1	1
rs7578597	1E-9	9	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	0	1	1	1
rs3134792	1E-9	9	18364390	Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene.	Psoriasis	0	1	1	1
rs17810546	1E-9	9	18311140	Newly identified genetic risk variants for celiac disease related to the immune response.	Celiac disease	0	0	1	1
rs6465657	1E-9	9	18264097	Multiple newly identified loci associated with prostate cancer susceptibility.	Prostate cancer	1	1	1	1
rs4430796	1E-9	9	18264096	Multiple loci identified in a genome-wide association study of prostate cancer.	Prostate cancer	0	0	1	1
rs562338	1E-9	9	18262040	LDL-cholesterol concentrations: a genome-wide association study.	LDL cholesterol	0	0	1	1
rs10499194	1E-9	9	17982456	Two independent alleles at 6q23 associated with risk of rheumatoid arthritis.	Rheumatoid arthritis	0	0	1	1
rs3096277	1E-9	9	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Blood pressure	1	1	1	1
rs7931462	2E-9	8.69897000433602	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (parent-of-origin)	1	1	1	1
rs10497324	2E-9	8.69897000433602	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (parent-of-origin)	1	1	1	1
rs10740993	2E-9	8.69897000433602	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (number of teeth)	0	1	1	1
rs12229918	2E-9	8.69897000433602	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (number of teeth)	0	1	0	0
rs412000	2E-9	8.69897000433602	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (time to first tooth eruption)	0	1	1	1
rs2067615	2E-9	8.69897000433602	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs7138803	2E-9	8.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Body mass index	0	0	0	0
rs2362965	2E-9	8.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs10838708	2E-9	8.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	1	1	1
rs780151	2E-9	8.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs4735692	2E-9	8.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs9568867	2E-9	8.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	1	1	1	1
rs6731302	2E-9	8.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	1	1	1	1
rs11208659	2E-9	8.69897000433602	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	1	1	1	1
rs564343	2E-9	8.69897000433602	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	1	1	1	1
rs11650494	2E-9	8.69897000433602	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs7241993	2E-9	8.69897000433602	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs10206899	2E-9	8.69897000433602	23535967	Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate.	Glomerular filtration rate	0	1	1	1
rs4859682	2E-9	8.69897000433602	23535967	Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate.	Glomerular filtration rate	0	1	1	1
rs1423386:rs6491679	2E-9	8.69897000433602	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs7714670:rs12880735	2E-9	8.69897000433602	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs9392653:rs7780976	2E-9	8.69897000433602	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs9804128:rs4784379	2E-9	8.69897000433602	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs1364505:rs1204660	2E-9	8.69897000433602	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs2288073:rs10771022	2E-9	8.69897000433602	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs1367228:rs3905075	2E-9	8.69897000433602	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs139371	2E-9	8.69897000433602	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (hyperdiploidy)	1	1	1	1
rs2272007	2E-9	8.69897000433602	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (hyperdiploidy)	0	0	0	0
rs17024684	2E-9	8.69897000433602	23471985	Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.	Brain connectivity	1	1	1	1
rs16997087	2E-9	8.69897000433602	23471985	Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.	Brain connectivity	0	0	0	0
rs7914558	2E-9	8.69897000433602	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs9287237	2E-9	8.69897000433602	23437003	Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure.	Bone mineral density	1	1	1	1
rs11624776	2E-9	8.69897000433602	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs17823642	2E-9	8.69897000433602	23378610	Genetic variants associated with glycine metabolism and their role in insulin sensitivity and type 2 diabetes.	Metabolite levels	0	1	1	1
rs6583437	2E-9	8.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs17348299	2E-9	8.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1122979	2E-9	8.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10813957	2E-9	8.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2621416	2E-9	8.69897000433602	23349640	Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.	Lymphoma	0	1	1	1
rs752092	2E-9	8.69897000433602	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs3213764	2E-9	8.69897000433602	23359319	Genome-wide association study identifies loci at ATF7IP and KLK2 associated with percentage of circulating free PSA.	Prostate-specific antigen levels	0	1	1	1
rs12518614	2E-9	8.69897000433602	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	1	1	1	1
rs9533425	2E-9	8.69897000433602	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	1	1	1	1
rs7188445	2E-9	8.69897000433602	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs7976059	2E-9	8.69897000433602	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs1435867	2E-9	8.69897000433602	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	1	1	1	1
rs1991866	2E-9	8.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs7210086	2E-9	8.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	1	1	1	1
rs1126510	2E-9	8.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	1	1	1	1
rs1537377	2E-9	8.69897000433602	23104006	Genome-wide association meta-analysis identifies new endometriosis risk loci.	Endometriosis	1	1	1	1
rs12437854	2E-9	8.69897000433602	23028342	New susceptibility loci associated with kidney disease in type 1 diabetes.	Type 1 diabetes nephropathy	1	1	1	1
rs17034687	2E-9	8.69897000433602	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs13026414	2E-9	8.69897000433602	22949513	Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32	Epilepsy (generalized)	1	1	1	1
rs4841132	2E-9	8.69897000433602	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	1	1	1
rs4676410	2E-9	8.69897000433602	22821403	Genome-wide association analysis in Primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4.	Sclerosing cholangitis and ulcerative colitis (combined)	0	1	1	1
rs7151526	2E-9	8.69897000433602	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	1	1	1	1
rs641153	2E-9	8.69897000433602	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (GA)	0	1	0	0
rs11191580	2E-9	8.69897000433602	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	0	1	1	1
rs12666575	2E-9	8.69897000433602	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	1	1	1	1
rs6945541	2E-9	8.69897000433602	22693459	Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.	Male-pattern baldness	1	1	1	1
rs5015480	2E-9	8.69897000433602	22693455	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.	Type 2 diabetes	0	0	1	1
rs6778194	2E-9	8.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	NA	NA	NA	NA
rs17331151	2E-9	8.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	0	0	0	0
rs174550	2E-9	8.69897000433602	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs10768122	2E-9	8.69897000433602	22561518	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.	Vitiligo	1	1	1	1
rs9568856	2E-9	8.69897000433602	22484627	A genome-wide association meta-analysis identifies new childhood obesity loci.	Obesity	0	0	1	1
rs9940128	2E-9	8.69897000433602	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs4910742	2E-9	8.69897000433602	22291609	A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.	Inflammatory biomarkers	0	1	1	1
rs2439302	2E-9	8.69897000433602	22267200	Discovery of common variants associated with low TSH levels and thyroid cancer risk.	Thyroid cancer	1	1	1	1
rs4521516	2E-9	8.69897000433602	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	1	1	1	1
rs397969	2E-9	8.69897000433602	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs1964516	2E-9	8.69897000433602	22080838	A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13.	Chronic obstructive pulmonary disease	0	0	1	1
rs7775228	2E-9	8.69897000433602	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	IgE grass sensitization	0	1	1	1
rs16856332	2E-9	8.69897000433602	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alkaline phosphatase)	1	1	1	1
rs2236653	2E-9	8.69897000433602	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alkaline phosphatase)	1	1	1	1
rs2739330	2E-9	8.69897000433602	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs2782980	2E-9	8.69897000433602	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	1	1	1	1
rs12368653	2E-9	8.69897000433602	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	0	1	1
rs7522462	2E-9	8.69897000433602	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs9469003	2E-9	8.69897000433602	21801394	Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.	Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS-TEN)	0	1	1	1
rs2521572	2E-9	8.69897000433602	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs1043879	2E-9	8.69897000433602	21700265	Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate.	Erythrocyte sedimentation rate	0	0	0	0
rs7527798	2E-9	8.69897000433602	21700265	Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate.	Erythrocyte sedimentation rate	0	0	0	0
rs2749097	2E-9	8.69897000433602	21665994	Genome-wide association study identifies two loci strongly affecting transferrin glycosylation.	Alcohol consumption (transferrin glycosylation)	1	1	1	1
rs744373	2E-9	8.69897000433602	21627779	The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease.	Alzheimer's disease	0	0	1	1
rs6010620	2E-9	8.69897000433602	21531791	Chromosome 7p11.2 (EGFR) variation influences glioma risk.	Glioma	0	0	1	1
rs3865444	2E-9	8.69897000433602	21460841	Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.	Alzheimer's disease (late onset)	1	1	1	1
rs1800693	2E-9	8.69897000433602	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	0	1	1	1
rs295	2E-9	8.69897000433602	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome	0	0	0	0
rs2266788	2E-9	8.69897000433602	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome	0	0	0	0
rs2075290	2E-9	8.69897000433602	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome	0	0	0	0
rs1387153	2E-9	8.69897000433602	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	0	0	0
rs2197089	2E-9	8.69897000433602	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	0	0	0
rs1919128	2E-9	8.69897000433602	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Waist Circumference - Triglycerides (WC-TG)	0	0	0	0
rs10479334	2E-9	8.69897000433602	21368711	Genome-wide association study of personality traits in bipolar patients.	Personality dimensions	1	1	1	1
rs1064395	2E-9	8.69897000433602	21353194	Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.	Bipolar disorder	1	1	1	1
rs1800961	2E-9	8.69897000433602	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	0	1	1	1
rs7579899	2E-9	8.69897000433602	21131975	Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3.	Renal cell carcinoma	1	1	1	1
rs11167764	2E-9	8.69897000433602	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs2872507	2E-9	8.69897000433602	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs17020136	2E-9	8.69897000433602	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs6687758	2E-9	8.69897000433602	20972440	Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.	Colorectal cancer	0	0	0	0
rs6861681	2E-9	8.69897000433602	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	0	1	1	1
rs4836133	2E-9	8.69897000433602	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs2899472	2E-9	8.69897000433602	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	AB1-42	1	1	1	1
rs16964211	2E-9	8.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs9456307	2E-9	8.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs6714546	2E-9	8.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	0	1	1
rs9472414	2E-9	8.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1013209	2E-9	8.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs6959212	2E-9	8.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs6879260	2E-9	8.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs10863936	2E-9	8.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs17806888	2E-9	8.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2353398	2E-9	8.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	0	0	0
rs2724475	2E-9	8.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	0	1	1
rs8170	2E-9	8.69897000433602	20852631	A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population.	Breast cancer	0	0	1	1
rs939658	2E-9	8.69897000433602	20835236	A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.	Refractive error	0	0	1	1
rs1495741	2E-9	8.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs2972146	2E-9	8.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	1	1
rs11065987	2E-9	8.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs2255141	2E-9	8.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs9303277	2E-9	8.69897000433602	20639880	Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis.	Primary biliary cirrhosis	0	1	1	1
rs174547	2E-9	8.69897000433602	20639392	Genome-wide association analysis identifies multiple loci related to resting heart rate.	Resting heart rate	0	1	1	1
rs11634397	2E-9	8.69897000433602	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	1	1	1	1
rs1470579	2E-9	8.69897000433602	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	0	0	1	1
rs6465825	2E-9	8.69897000433602	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs4819388	2E-9	8.69897000433602	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs35767	2E-9	8.69897000433602	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	1	1	1
rs35767	2E-9	8.69897000433602	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting insulin-related traits	0	1	0	0
rs2251219	2E-9	8.69897000433602	20081856	Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.	Major mood disorders	0	1	1	1
rs757978	2E-9	8.69897000433602	20062064	Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk.	Chronic lymphocytic leukemia	1	1	1	1
rs676210	2E-9	8.69897000433602	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs2412973	2E-9	8.69897000433602	19915574	Common variants at five new loci associated with early-onset inflammatory bowel disease.	Inflammatory bowel disease (early onset)	0	1	1	1
rs8049439	2E-9	8.69897000433602	19915574	Common variants at five new loci associated with early-onset inflammatory bowel disease.	Inflammatory bowel disease (early onset)	0	1	1	1
rs1800562	2E-9	8.69897000433602	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Hematocrit	0	1	0	0
rs16921914	2E-9	8.69897000433602	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	1	1	1	1
rs651164	2E-9	8.69897000433602	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	NA	NA	NA	NA
rs4026608	2E-9	8.69897000433602	19584346	Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.	Aortic root size	1	1	1	1
rs2284063	2E-9	8.69897000433602	19578364	Genome-wide association study identifies three loci associated with melanoma risk.	Melanoma	1	1	1	1
rs4809324	2E-9	8.69897000433602	19578366	Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.	Glioma (high-grade)	1	1	1	1
rs12807809	2E-9	8.69897000433602	19571808	Common variants conferring risk of schizophrenia.	Schizophrenia	1	1	1	1
rs505802	2E-9	8.69897000433602	19503597	Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.	Uric acid levels	0	0	0	0
rs2090409	2E-9	8.69897000433602	19448620	Meta-analysis of genome-wide association data identifies two loci influencing age at menarche.	Menarche (age at onset)	0	0	1	1
rs11203203	2E-9	8.69897000433602	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs3024505	2E-9	8.69897000433602	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs381815	2E-9	8.69897000433602	19430479	Genome-wide association study of blood pressure and hypertension.	Systolic blood pressure	1	1	1	1
rs1122608	2E-9	8.69897000433602	19198609	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.	Myocardial infarction (early onset)	0	1	1	1
rs439401	2E-9	8.69897000433602	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Triglycerides	0	0	0	0
rs9309413	2E-9	8.69897000433602	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	0	1	1	1
rs9298506	2E-9	8.69897000433602	18997786	Susceptibility loci for intracranial aneurysm in European and Japanese populations.	Intracranial aneurysm	0	0	1	1
rs6920220	2E-9	8.69897000433602	18794853	Common variants at CD40 and other loci confer risk of rheumatoid arthritis.	Rheumatoid arthritis	0	0	1	1
rs4149056	2E-9	8.69897000433602	18650507	SLCO1B1 variants and statin-induced myopathy--a genomewide study.	Response to statin therapy	0	1	1	1
rs9286879	2E-9	8.69897000433602	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs17582416	2E-9	8.69897000433602	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs3760318	2E-9	8.69897000433602	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs6854783	2E-9	8.69897000433602	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs5945619	2E-9	8.69897000433602	18264097	Multiple newly identified loci associated with prostate cancer susceptibility.	Prostate cancer	NA	NA	NA	NA
rs10896449	2E-9	8.69897000433602	18264096	Multiple loci identified in a genome-wide association study of prostate cancer.	Prostate cancer	0	0	1	1
rs1412337	2E-9	8.69897000433602	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Morbidity-free survival	1	1	1	1
rs32566	2E-9	8.69897000433602	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Morbidity-free survival	1	1	1	1
rs4402960	2E-9	8.69897000433602	17463246	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	Type 2 diabetes	0	0	1	1
rs9905704	3E-9	8.52287874528034	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	0	0	1	1
rs4075154	3E-9	8.52287874528034	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs2322633	3E-9	8.52287874528034	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs11209718	3E-9	8.52287874528034	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs1516725	3E-9	8.52287874528034	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs2370983	3E-9	8.52287874528034	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs514716	3E-9	8.52287874528034	23562540	GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.	Alzheimer's disease biomarkers	1	1	1	1
rs132390	3E-9	8.52287874528034	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs1805007	3E-9	8.52287874528034	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Hair color	0	0	0	0
rs536477:rs1937920	3E-9	8.52287874528034	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs2710201:rs3780293	3E-9	8.52287874528034	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs12541254:rs305009	3E-9	8.52287874528034	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs2235529	3E-9	8.52287874528034	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	0	0	1	1
rs9834692	3E-9	8.52287874528034	23471985	Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.	Brain connectivity	1	1	1	1
rs9883474	3E-9	8.52287874528034	23471985	Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.	Brain connectivity	0	0	0	0
rs3771863	3E-9	8.52287874528034	23471985	Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.	Brain connectivity	1	1	1	1
rs7628864	3E-9	8.52287874528034	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs10994359	3E-9	8.52287874528034	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs7825175	3E-9	8.52287874528034	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	1	1	1
rs174541	3E-9	8.52287874528034	23378610	Genetic variants associated with glycine metabolism and their role in insulin sensitivity and type 2 diabetes.	Metabolite levels	0	0	1	1
rs909674	3E-9	8.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10813957	3E-9	8.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11119805 	3E-9	8.52287874528034	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Stearic acid (18:0) plasma levels	NA	NA	NA	NA
rs7982677	3E-9	8.52287874528034	23297363	Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.	Tetralogy of Fallot	1	1	1	1
rs7594321	3E-9	8.52287874528034	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	0	0	0
rs7312105	3E-9	8.52287874528034	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs2572207	3E-9	8.52287874528034	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs11650106	3E-9	8.52287874528034	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity and mass	0	1	1	1
rs17391694	3E-9	8.52287874528034	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	0	1	1	1
rs254560	3E-9	8.52287874528034	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	0	0	1	1
rs12216812	3E-9	8.52287874528034	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs204999	3E-9	8.52287874528034	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum total protein level	0	0	0	0
rs12507628	3E-9	8.52287874528034	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	1	1	1	1
rs8031948	3E-9	8.52287874528034	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	0	1	1	1
rs440837	3E-9	8.52287874528034	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	1	1	1	1
rs7089814	3E-9	8.52287874528034	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs6028	3E-9	8.52287874528034	22703881	Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.	Activated partial thromboplastin time	0	1	1	1
rs10502861	3E-9	8.52287874528034	22693459	Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.	Male-pattern baldness	1	1	1	1
rs4402960	3E-9	8.52287874528034	22693455	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.	Type 2 diabetes	0	0	1	1
rs2272205	3E-9	8.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs17142462	3E-9	8.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-12p40)	1	1	1	1
rs12247397	3E-9	8.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-1beta)	NA	NA	NA	NA
rs11118316	3E-9	8.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	1	1	1
rs11248060	3E-9	8.52287874528034	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	0	0	1	1
rs7937	3E-9	8.52287874528034	22080838	A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13.	Chronic obstructive pulmonary disease	0	1	1	1
rs6834314	3E-9	8.52287874528034	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alanine transaminase)	0	1	1	1
rs174601	3E-9	8.52287874528034	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alkaline phosphatase)	0	1	1	1
rs9296736	3E-9	8.52287874528034	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs17145750	3E-9	8.52287874528034	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	0	1	1	1
rs4581712	3E-9	8.52287874528034	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs1801516	3E-9	8.52287874528034	21983787	Genome-wide association study identifies three new melanoma susceptibility loci.	Melanoma	1	1	1	1
rs45430	3E-9	8.52287874528034	21983787	Genome-wide association study identifies three new melanoma susceptibility loci.	Melanoma	1	1	1	1
rs4790333	3E-9	8.52287874528034	21873549	Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.	Proinsulin levels	0	1	1	1
rs11212617	3E-9	8.52287874528034	21845381	Does metformin work for everyone? A genome-wide association study for metformin response.	Response to metformin	0	1	1	1
rs2293370	3E-9	8.52287874528034	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs7238078	3E-9	8.52287874528034	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs198426	3E-9	8.52287874528034	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs7584330	3E-9	8.52287874528034	21743467	Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.	Prostate cancer	1	1	1	1
rs7524102	3E-9	8.52287874528034	21732829	Wnt signaling and Dupuytren's disease.	Dupuytren's disease	0	1	1	1
rs536841	3E-9	8.52287874528034	21627779	The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease.	Alzheimer's disease	0	0	1	1
rs11884476	3E-9	8.52287874528034	21502085	Genome-wide association study implicates PARD3B-based AIDS restriction.	AIDS progression	1	1	1	1
rs11624704	3E-9	8.52287874528034	21552555	A genome-wide association study on obesity and obesity-related traits.	Obesity	1	1	1	1
rs11823543	3E-9	8.52287874528034	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Triglycerides-Blood Pressure (TG-BP)	0	1	0	0
rs11825181	3E-9	8.52287874528034	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Triglycerides-Blood Pressure (TG-BP)	0	0	0	0
rs734999	3E-9	8.52287874528034	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	0	1	1
rs6451493	3E-9	8.52287874528034	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs1799945	3E-9	8.52287874528034	21208937	Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.	Iron levels	0	1	1	1
rs11212617	3E-9	8.52287874528034	21186350	Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes.	Response to metformin	0	0	1	1
rs391525	3E-9	8.52287874528034	21131588	Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL.	Chronic lymphocytic leukemia	0	1	1	1
rs7821178	3E-9	8.52287874528034	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	0	1	1	1
rs12722489	3E-9	8.52287874528034	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs29941	3E-9	8.52287874528034	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	0	1	1
rs4929949	3E-9	8.52287874528034	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	1	1	1
rs1741344	3E-9	8.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs7909670	3E-9	8.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1800562	3E-9	8.52287874528034	20927387	A genome-wide association study of red blood cell traits using the electronic medical record.	Red blood cell traits	0	0	1	1
rs3771166	3E-9	8.52287874528034	20860503	A large-scale, consortium-based genomewide association study of asthma.	Asthma	0	0	1	1
rs2779116	3E-9	8.52287874528034	20858683	Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.	Glycated hemoglobin levels	0	1	1	1
rs10088218	3E-9	8.52287874528034	20852632	A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.	Ovarian cancer	0	0	1	1
rs11248051	3E-9	8.52287874528034	20711177	Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.	Parkinson's disease	0	0	1	1
rs3757354	3E-9	8.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs581080	3E-9	8.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs737337	3E-9	8.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs9488822	3E-9	8.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs849134	3E-9	8.52287874528034	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	0	0	1	1
rs1393350	3E-9	8.52287874528034	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Eye color	0	0	0	0
rs4810485	3E-9	8.52287874528034	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs706779	3E-9	8.52287874528034	20410501	Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.	Vitiligo	0	1	1	1
rs2056626	3E-9	8.52287874528034	20383147	Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.	Systemic sclerosis	0	1	1	1
rs3821236	3E-9	8.52287874528034	20383147	Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.	Systemic sclerosis	0	0	1	1
rs9315204	3E-9	8.52287874528034	20364137	Genome-wide association study of intracranial aneurysm identifies three new risk loci.	Intracranial aneurysm	1	1	1	1
rs10800309	3E-9	8.52287874528034	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	0	0	1	1
rs3806932	3E-9	8.52287874528034	20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Eosinophilic esophagitis (pediatric)	1	1	1	1
rs3748816	3E-9	8.52287874528034	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs13314993	3E-9	8.52287874528034	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	1	1	1	1
rs9792269	3E-9	8.52287874528034	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs1801222	3E-9	8.52287874528034	19744961	Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.	Folate pathway vitamin levels	1	1	1	1
rs4975616	3E-9	8.52287874528034	19654303	Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.	Lung cancer	0	1	1	1
rs6010620	3E-9	8.52287874528034	19578366	Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.	Glioma (high-grade)	0	1	1	1
rs6717918	3E-9	8.52287874528034	19570815	A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.	Height	0	0	1	1
rs12129861	3E-9	8.52287874528034	19503597	Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.	Uric acid levels	0	1	1	1
rs7861820	3E-9	8.52287874528034	19448621	Genome-wide association studies identify loci associated with age at menarche and age at natural menopause.	Menarche and menopause (age at onset)	0	1	1	1
rs9815354	3E-9	8.52287874528034	19430479	Genome-wide association study of blood pressure and hypertension.	Diastolic blood pressure	0	1	1	1
rs1182188	3E-9	8.52287874528034	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs11648785	3E-9	8.52287874528034	19340012	Genome-wide association study of tanning phenotype in a population of European ancestry.	Tanning	0	1	1	1
rs6987702	3E-9	8.52287874528034	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	0	1	1
rs1148259	3E-9	8.52287874528034	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	1	1	1	1
rs10758669	3E-9	8.52287874528034	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs737267	3E-9	8.52287874528034	18327257	SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout.	Urate levels	0	0	1	1
rs16996148	3E-9	8.52287874528034	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	LDL cholesterol	0	0	1	1
rs16996148	3E-9	8.52287874528034	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	Triglycerides	0	0	0	0
rs3817198	3E-9	8.52287874528034	17529967	Genome-wide association study identifies novel breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs1799922	4E-9	8.39794000867204	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (number of teeth)	1	1	1	1
rs8046148	4E-9	8.39794000867204	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	1	1	1	1
rs12940923	4E-9	8.39794000867204	23620142	Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.	Circulating myeloperoxidase levels (plasma)	0	1	1	1
rs826838	4E-9	8.39794000867204	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs10231759	4E-9	8.39794000867204	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	1	1	1
rs4953076	4E-9	8.39794000867204	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs2112347	4E-9	8.39794000867204	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs11639988	4E-9	8.39794000867204	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs11109072	4E-9	8.39794000867204	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	1	1	1	1
rs4911414	4E-9	8.39794000867204	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Tanning	1	1	1	1
rs4507975:rs9914518	4E-9	8.39794000867204	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs2771051:rs827637	4E-9	8.39794000867204	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs10516089:rs11072930	4E-9	8.39794000867204	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs10504130:rs2847351	4E-9	8.39794000867204	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs10500355	4E-9	8.39794000867204	23474815	Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.	Refractive error	0	0	1	1
rs7759938	4E-9	8.39794000867204	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs9371601	4E-9	8.39794000867204	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs7744813	4E-9	8.39794000867204	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs2186369	4E-9	8.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11763147	4E-9	8.39794000867204	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs4938174	4E-9	8.39794000867204	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs1034200	4E-9	8.39794000867204	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs10480300	4E-9	8.39794000867204	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs7764819	4E-9	8.39794000867204	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs1801253	4E-9	8.39794000867204	23202124	New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.	Birth weight	0	1	1	1
rs864745	4E-9	8.39794000867204	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	0	1	1	1
rs16967103	4E-9	8.39794000867204	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs4743820	4E-9	8.39794000867204	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs12700667	4E-9	8.39794000867204	23104006	Genome-wide association meta-analysis identifies new endometriosis risk loci.	Endometriosis	0	0	1	1
rs694419	4E-9	8.39794000867204	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	1	1	1	1
rs9257809	4E-9	8.39794000867204	22961001	Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.	Barrett's esophagus	1	1	1	1
rs3798722	4E-9	8.39794000867204	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	1	1	1
rs6511720	4E-9	8.39794000867204	22916037	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Metabolite levels	0	1	1	1
rs2736100	4E-9	8.39794000867204	22886559	Genome-wide association study of glioma and meta-analysis.	Glioma	0	0	1	1
rs11766298	4E-9	8.39794000867204	22890011	Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate.	Response to fenofibrate	1	1	1	1
rs7733088	4E-9	8.39794000867204	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	0	1	1	1
rs9525638	4E-9	8.39794000867204	22792071	WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk.	Cortical thickness	1	1	1	1
rs9408928	4E-9	8.39794000867204	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	0	1	1	1
rs17000918	4E-9	8.39794000867204	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-1beta)	NA	NA	NA	NA
rs340874	4E-9	8.39794000867204	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs10824026	4E-9	8.39794000867204	22544366	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	Atrial fibrillation	0	1	1	1
rs9299	4E-9	8.39794000867204	22484627	A genome-wide association meta-analysis identifies new childhood obesity loci.	Obesity	0	1	1	1
rs867186	4E-9	8.39794000867204	22216198	A genome-wide association study of the Protein C anticoagulant pathway.	Anticoagulant levels	0	1	1	1
rs3792366	4E-9	8.39794000867204	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs10883437	4E-9	8.39794000867204	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alanine transaminase)	0	1	1	1
rs7850258	4E-9	8.39794000867204	21981779	Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.	Hypothyroidism	0	0	1	1
rs478222	4E-9	8.39794000867204	21980299	A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.	Type 1 diabetes	0	1	1	1
rs11754288	4E-9	8.39794000867204	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	1	1	1
rs13082711	4E-9	8.39794000867204	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	0	1	1	1
rs2071518	4E-9	8.39794000867204	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	1	1	1	1
rs1173771	4E-9	8.39794000867204	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs3120139	4E-9	8.39794000867204	21900290	Genetic variants, plasma lipoprotein(a) levels, and risk of cardiovascular morbidity and mortality among two prospective cohorts of type 2 diabetes.	Lp (a) levels	0	0	0	0
rs382140	4E-9	8.39794000867204	21876539	Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM.	Coffee consumption	1	1	1	1
rs2651899	4E-9	8.39794000867204	21666692	Genome-wide association study reveals three susceptibility loci for common migraine in the general population.	Migraine	1	1	1	1
rs11172113	4E-9	8.39794000867204	21666692	Genome-wide association study reveals three susceptibility loci for common migraine in the general population.	Migraine	0	1	1	1
rs4773144	4E-9	8.39794000867204	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	1	1	1	1
rs340029	4E-9	8.39794000867204	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	0	1	1	1
rs13233571	4E-9	8.39794000867204	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	0	1	1	1
rs1659127	4E-9	8.39794000867204	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	0	1	1	1
rs2476601	4E-9	8.39794000867204	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs6738825	4E-9	8.39794000867204	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	1	1	1	1
rs702873	4E-9	8.39794000867204	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	0	1	1	1
rs280519	4E-9	8.39794000867204	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	0	0	0	0
rs9844666	4E-9	8.39794000867204	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs744910	4E-9	8.39794000867204	20860503	A large-scale, consortium-based genomewide association study of asthma.	Asthma	0	1	1	1
rs10489615	4E-9	8.39794000867204	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs1034200	4E-9	8.39794000867204	20719862	New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.	Central corneal thickness	0	1	1	1
rs2290159	4E-9	8.39794000867204	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	1	1	1	1
rs2814944	4E-9	8.39794000867204	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	0	0
rs2081687	4E-9	8.39794000867204	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs7206971	4E-9	8.39794000867204	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	1	1	1	1
rs735665	4E-9	8.39794000867204	20639881	Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.	Follicular lymphoma	0	1	1	1
rs1531343	4E-9	8.39794000867204	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	1	1	1	1
rs17265703	4E-9	8.39794000867204	20558539	Common genetic variants associate with serum phosphorus concentration.	Phosphorus levels	0	1	1	1
rs2970818	4E-9	8.39794000867204	20558539	Common genetic variants associate with serum phosphorus concentration.	Phosphorus levels	1	1	1	1
rs17146964	4E-9	8.39794000867204	20548946	A genome-wide association study of optic disc parameters.	Vertical cup-disc ratio	0	1	1	1
rs704010	4E-9	8.39794000867204	20453838	Genome-wide association study identifies five new breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs9621532	4E-9	8.39794000867204	20385826	Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).	Age-related macular degeneration	NA	NA	NA	NA
rs3197999	4E-9	8.39794000867204	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	0	0	1	1
rs296547	4E-9	8.39794000867204	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs2115763	4E-9	8.39794000867204	20150558	Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels.	Interleukin-18 levels	0	1	1	1
rs6795970	4E-9	8.39794000867204	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	0	0	0
rs3995090	4E-9	8.39794000867204	20010834	Genome-wide association study identifies five loci associated with lung function.	Pulmonary function	0	0	1	1
rs2304256	4E-9	8.39794000867204	19966805	The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs1167998	4E-9	8.39794000867204	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs7932354	4E-9	8.39794000867204	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (hip)	0	1	1	1
rs9960767	4E-9	8.39794000867204	19571808	Common variants conferring risk of schizophrenia.	Schizophrenia	1	1	1	1
rs17445836	4E-9	8.39794000867204	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	0	1	1	1
rs17824933	4E-9	8.39794000867204	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs4900384	4E-9	8.39794000867204	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs7647305	4E-9	8.39794000867204	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	1	0	0
rs925946	4E-9	8.39794000867204	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	1	0	0
rs7679	4E-9	8.39794000867204	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	HDL cholesterol	0	0	0	0
rs6102059	4E-9	8.39794000867204	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	LDL cholesterol	1	1	1	1
rs947474	4E-9	8.39794000867204	18978792	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.	Type 1 diabetes	1	1	1	1
rs11083846	4E-9	8.39794000867204	18758461	A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia.	Chronic lymphocytic leukemia	0	1	1	1
rs4800148	4E-9	8.39794000867204	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs13015714	4E-9	8.39794000867204	18311140	Newly identified genetic risk variants for celiac disease related to the immune response.	Celiac disease	0	0	1	1
rs16996148	4E-9	8.39794000867204	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	Triglycerides	0	0	1	1
rs599839	4E-9	8.39794000867204	17634449	Genomewide association analysis of coronary artery disease.	Coronary heart disease	0	0	1	1
rs1004446	4E-9	8.39794000867204	17632545	A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.	Type 1 diabetes	0	0	1	1
rs965808	5E-9	8.30102999566398	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	1	1	1	1
rs13401104	5E-9	8.30102999566398	23722424	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.	Educational attainment	1	1	1	1
rs9967417	5E-9	8.30102999566398	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs1514177	5E-9	8.30102999566398	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs9877502	5E-9	8.30102999566398	23562540	GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.	Alzheimer's disease biomarkers	1	1	1	1
rs3771570	5E-9	8.30102999566398	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	0	1	1	1
rs3096702	5E-9	8.30102999566398	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	0	1	1	1
rs2046210	5E-9	8.30102999566398	23544013	Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.	Breast Cancer in BRCA1 mutation carriers	0	1	1	1
rs318497:rs7019259	5E-9	8.30102999566398	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs6695223:rs1763510	5E-9	8.30102999566398	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs1336708:rs1423386	5E-9	8.30102999566398	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs6771316:rs10986432	5E-9	8.30102999566398	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs10485022	5E-9	8.30102999566398	23471985	Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.	Brain connectivity	0	0	0	0
rs6795735	5E-9	8.30102999566398	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	0	1	1	1
rs1006737	5E-9	8.30102999566398	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs12229663	5E-9	8.30102999566398	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs11726248	5E-9	8.30102999566398	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs753760	5E-9	8.30102999566398	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs6583437	5E-9	8.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7078012	5E-9	8.30102999566398	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	0	0	0
rs1923539	5E-9	8.30102999566398	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	0	0	0
rs17695092	5E-9	8.30102999566398	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	0	0	1	1
rs727088	5E-9	8.30102999566398	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs4737395	5E-9	8.30102999566398	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs1472750	5E-9	8.30102999566398	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs9399137	5E-9	8.30102999566398	23043469	HbA2 levels in normal adults are influenced by two distinct genetic mechanisms.	HbA2 levels	0	1	1	1
rs3792109	5E-9	8.30102999566398	22936669	A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.	Crohn's disease	0	0	1	1
rs5954596	5E-9	8.30102999566398	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	NA	NA	NA	NA
rs11177	5E-9	8.30102999566398	22763110	Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study.	Osteoarthritis	0	1	1	1
rs17483466	5E-9	8.30102999566398	22700719	Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.	Chronic lymphocytic leukemia	0	0	1	1
rs13231718	5E-9	8.30102999566398	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-10)	1	1	1	1
rs4691380	5E-9	8.30102999566398	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	1	1	1	1
rs13003464	5E-9	8.30102999566398	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	0	1	1	1
rs11591147	5E-9	8.30102999566398	22331829	Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial.	Response to statin therapy (LDL-C)	0	1	1	1
rs61839660	5E-9	8.30102999566398	22293688	1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.	Type 1 diabetes	0	0	1	1
rs7911500	5E-9	8.30102999566398	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	0	1	1	1
rs6448771	5E-9	8.30102999566398	22028671	A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol.	Lipid traits	1	1	1	1
rs2954021	5E-9	8.30102999566398	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alanine transaminase)	0	1	0	0
rs7186908	5E-9	8.30102999566398	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (alkaline phosphatase)	0	1	1	1
rs9663362	5E-9	8.30102999566398	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs13082711	5E-9	8.30102999566398	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs1173771	5E-9	8.30102999566398	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	0	0	0
rs2303759	5E-9	8.30102999566398	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs7923837	5E-9	8.30102999566398	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs2283792	5E-9	8.30102999566398	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs2019960	5E-9	8.30102999566398	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs354033	5E-9	8.30102999566398	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs1109748	5E-9	8.30102999566398	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs902774	5E-9	8.30102999566398	21743057	Genome-wide association study identifies new prostate cancer susceptibility loci.	Prostate cancer	1	1	1	1
rs2233287	5E-9	8.30102999566398	21750679	Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.	Systemic sclerosis	0	1	1	1
rs2497306	5E-9	8.30102999566398	21533175	Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.	Dehydroepiandrosterone sulphate levels	0	1	1	1
rs10790162	5E-9	8.30102999566398	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome	0	0	0	0
rs13022873	5E-9	8.30102999566398	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Waist Circumference - Triglycerides (WC-TG)	0	0	0	0
rs35675666	5E-9	8.30102999566398	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs700752	5E-9	8.30102999566398	21216879	A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3.	Insulin-like growth factors	0	0	0	0
rs17342717	5E-9	8.30102999566398	21208937	Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.	Iron levels	0	1	1	1
rs1847472	5E-9	8.30102999566398	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs6699417	5E-9	8.30102999566398	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs1330	5E-9	8.30102999566398	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs855791	5E-9	8.30102999566398	20927387	A genome-wide association study of red blood cell traits using the electronic medical record.	Red blood cell traits	0	0	0	0
rs3894194	5E-9	8.30102999566398	20860503	A large-scale, consortium-based genomewide association study of asthma.	Asthma	0	0	1	1
rs7998202	5E-9	8.30102999566398	20858683	Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.	Glycated hemoglobin levels	1	1	1	1
rs4129767	5E-9	8.30102999566398	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs1362756	5E-9	8.30102999566398	20548946	A genome-wide association study of optic disc parameters.	Optic disc parameters	1	1	1	1
rs889312	5E-9	8.30102999566398	20453838	Genome-wide association study identifies five new breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs4820268	5E-9	8.30102999566398	19880490	A genome-wide association analysis of serum iron concentrations.	Iron levels	0	0	1	1
rs7804356	5E-9	8.30102999566398	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs3184504	5E-9	8.30102999566398	19430479	Genome-wide association study of blood pressure and hypertension.	Systolic blood pressure	0	1	0	0
rs16948048	5E-9	8.30102999566398	19430483	Genome-wide association study identifies eight loci associated with blood pressure.	Diastolic blood pressure	0	1	1	1
rs6830062	5E-9	8.30102999566398	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs10831496	5E-9	8.30102999566398	19340012	Genome-wide association study of tanning phenotype in a population of European ancestry.	Tanning	1	1	1	1
rs29941	5E-9	8.30102999566398	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	1	0	0
rs10838738	5E-9	8.30102999566398	19079261	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.	Body mass index	0	0	1	1
rs10411210	5E-9	8.30102999566398	19011631	Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer.	Colorectal cancer	1	1	1	1
rs1456893	5E-9	8.30102999566398	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	1	1	1
rs1551398	5E-9	8.30102999566398	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs2872507	5E-9	8.30102999566398	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs1038304	5E-9	8.30102999566398	18445777	Multiple genetic loci for bone mineral density and fractures.	Bone mineral density (hip)	0	0	0	0
rs1390401	5E-9	8.30102999566398	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs1464510	5E-9	8.30102999566398	18311140	Newly identified genetic risk variants for celiac disease related to the immune response.	Celiac disease	0	0	1	1
rs12699477	6E-9	8.22184874961636	23666239	Meta-analysis identifies four new loci associated with testicular germ cell tumor.	Testicular germ cell tumor	0	1	1	1
rs13130484	6E-9	8.22184874961636	23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Body mass index	0	0	1	1
rs887912	6E-9	8.22184874961636	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs9303542	6E-9	8.22184874961636	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	0	0	0	0
rs11782652	6E-9	8.22184874961636	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	0	0	0	0
rs10206899	6E-9	8.22184874961636	23535967	Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate.	Glomerular filtration rate	0	0	0	0
rs533259	6E-9	8.22184874961636	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs11601239	6E-9	8.22184874961636	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs11190604 	6E-9	8.22184874961636	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	NA	NA	NA	NA
rs1265093	6E-9	8.22184874961636	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	0	0	0
rs7527939	6E-9	8.22184874961636	23142968	Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene.	Schizophrenia	1	1	1	1
rs13394619	6E-9	8.22184874961636	23104006	Genome-wide association meta-analysis identifies new endometriosis risk loci.	Endometriosis	1	1	1	1
rs2280401	6E-9	8.22184874961636	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	1	1	1	1
rs13041247	6E-9	8.22184874961636	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs10033900	6E-9	8.22184874961636	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (CNV)	0	1	1	1
rs6576443	6E-9	8.22184874961636	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs238295	6E-9	8.22184874961636	22343285	Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans.	Cortical structure	1	1	1	1
rs2304130	6E-9	8.22184874961636	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Sphingolipid levels	0	1	1	1
rs2300747	6E-9	8.22184874961636	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs3811444	6E-9	8.22184874961636	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs10822013	6E-9	8.22184874961636	21908515	Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium.	Breast cancer	1	1	1	1
rs802734	6E-9	8.22184874961636	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs1250550	6E-9	8.22184874961636	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs10809650	6E-9	8.22184874961636	21732829	Wnt signaling and Dupuytren's disease.	Dupuytren's disease	1	1	1	1
rs11820589	6E-9	8.22184874961636	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	1	0	0
rs12531711	6E-9	8.22184874961636	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	0	0	0	0
rs10423674	6E-9	8.22184874961636	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs4687718	6E-9	8.22184874961636	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs11789399	6E-9	8.22184874961636	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs7178424	6E-9	8.22184874961636	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs6569992	6E-9	8.22184874961636	20927387	A genome-wide association study of red blood cell traits using the electronic medical record.	Red blood cell traits	0	0	0	0
rs9992101	6E-9	8.22184874961636	20383145	Genetic loci influencing kidney function and chronic kidney disease.	Creatinine levels	0	1	1	1
rs4675374	6E-9	8.22184874961636	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs10506525	6E-9	8.22184874961636	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (time to first tooth eruption)	0	0	1	1
rs8099917	6E-9	8.22184874961636	20060832	Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study.	Chronic Hepatitis C infection	0	1	1	1
rs1250550	6E-9	8.22184874961636	19915574	Common variants at five new loci associated with early-onset inflammatory bowel disease.	Inflammatory bowel disease (early onset)	0	1	1	1
rs1537415	6E-9	8.22184874961636	19897590	A genome-wide association study identifies GLT6D1 as a susceptibility locus for periodontitis.	Periodontitis	1	1	1	1
rs231735	6E-9	8.22184874961636	19503088	REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.	Rheumatoid arthritis	0	1	1	1
rs2736340	6E-9	8.22184874961636	19503088	REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.	Rheumatoid arthritis	0	1	1	1
rs12474609	6E-9	8.22184874961636	19367585	A genome screen of successful aging without cognitive decline identifies LRP1B by haplotype analysis.	Aging	1	1	1	1
rs12670798	6E-9	8.22184874961636	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	LDL cholesterol	0	0	1	1
rs1975197	6E-9	8.22184874961636	18660810	PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome.	Restless legs syndrome	0	0	1	1
rs7112513	6E-9	8.22184874961636	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	1	1	1
rs1278769	7E-9	8.15490195998574	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	1	1	1	1
rs4337252	7E-9	8.15490195998574	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs7184597	7E-9	8.15490195998574	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs2820464	7E-9	8.15490195998574	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Waist-hip ratio	0	0	1	1
rs11242675	7E-9	8.15490195998574	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs10069690	7E-9	8.15490195998574	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	0	0	1	1
rs664910:rs877228	7E-9	8.15490195998574	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs9945428:rs4823535	7E-9	8.15490195998574	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs1910358:rs9981595	7E-9	8.15490195998574	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs10994397	7E-9	8.15490195998574	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	0	0	0
rs59007384	7E-9	8.15490195998574	23419831	APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.	Alzheimer's disease biomarkers	0	0	0	0
rs11145465	7E-9	8.15490195998574	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs404256	7E-9	8.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7929679	7E-9	8.15490195998574	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	1	1	1
rs4656958	7E-9	8.15490195998574	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs630923	7E-9	8.15490195998574	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs7142143	7E-9	8.15490195998574	23007406	Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs742071	7E-9	8.15490195998574	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs16850864	7E-9	8.15490195998574	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-1beta)	1	1	1	1
rs16850885	7E-9	8.15490195998574	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-1beta)	0	0	0	0
rs9841287	7E-9	8.15490195998574	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	1	1	1	1
rs7927044	7E-9	8.15490195998574	22560479	Genome-wide association study of the age of onset of childhood asthma.	Asthma (childhood onset)	1	1	1	1
rs2980879	7E-9	8.15490195998574	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	0	0	0
rs6545946	7E-9	8.15490195998574	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	1	1	1	1
rs7076156	7E-9	8.15490195998574	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	0	0	1	1
rs4924410	7E-9	8.15490195998574	22327514	Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma.	Ewing sarcoma	0	1	1	1
rs2164983	7E-9	8.15490195998574	22197932	Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis.	Atopic dermatitis	1	1	1	1
rs1335645	7E-9	8.15490195998574	22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Liver enzyme levels (gamma-glutamyl transferase)	1	1	1	1
rs7023329	7E-9	8.15490195998574	21983787	Genome-wide association study identifies three new melanoma susceptibility loci.	Melanoma	0	1	1	1
rs6495122	7E-9	8.15490195998574	21876539	Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM.	Coffee consumption	0	0	0	0
rs2736100	7E-9	8.15490195998574	21827660	Combinations of newly confirmed Glioma-Associated loci link regions on chromosomes 1 and 9 to increased disease risk.	Glioma	0	0	1	1
rs3764261	7E-9	8.15490195998574	21665990	Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs6710823	7E-9	8.15490195998574	21292315	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.	Parkinson's disease	1	1	1	1
rs674313	7E-9	8.15490195998574	21131588	Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL.	Chronic lymphocytic leukemia	0	1	1	1
rs2797685	7E-9	8.15490195998574	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	1	1	1	1
rs10181042	7E-9	8.15490195998574	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs13073817	7E-9	8.15490195998574	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs17309827	7E-9	8.15490195998574	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	1	1	1	1
rs3110496	7E-9	8.15490195998574	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs643531	7E-9	8.15490195998574	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs12967135	7E-9	8.15490195998574	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	1	1
rs1260326	7E-9	8.15490195998574	20657596	Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.	Hypertriglyceridemia	0	1	1	1
rs924080	7E-9	8.15490195998574	20622878	Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.	Behcet's disease	0	1	1	1
rs13003464	7E-9	8.15490195998574	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	0	0	1	1
rs9858542	7E-9	8.15490195998574	19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Ulcerative colitis	0	0	1	1
rs11995824	7E-9	8.15490195998574	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (hip)	0	0	0	0
rs2814707	7E-9	8.15490195998574	19734901	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	0	0	1	1
rs7759938	7E-9	8.15490195998574	19448620	Meta-analysis of genome-wide association data identifies two loci influencing age at menarche.	Menarche (age at onset)	0	0	1	1
rs1990760	7E-9	8.15490195998574	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	0	1	1
rs1746048	7E-9	8.15490195998574	19198609	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.	Myocardial infarction (early onset)	0	1	1	1
rs3806308	7E-9	8.15490195998574	19122664	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.	Ulcerative colitis	1	1	1	1
rs1736135	7E-9	8.15490195998574	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs3116602	7E-9	8.15490195998574	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs6445975	7E-9	8.15490195998574	18204446	Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.	Systemic lupus erythematosus	1	1	1	1
rs1906953	8E-9	8.09691001300806	23727862	Genome-wide association study identifies two susceptibility loci for osteosarcoma.	Osteosarcoma	1	1	1	1
rs2273669	8E-9	8.09691001300806	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs643507	8E-9	8.09691001300806	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (asthmatics)	1	1	1	1
rs204247	8E-9	8.09691001300806	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs17530068	8E-9	8.09691001300806	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs8321	8E-9	8.09691001300806	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	0	0	0
rs6421315	8E-9	8.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs838133	8E-9	8.09691001300806	23372041	Novel locus including FGF21 is associated with dietary macronutrient intake.	Dietary macronutrient intake	0	0	1	1
rs1324183	8E-9	8.09691001300806	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs2571445	8E-9	8.09691001300806	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs7529925	8E-9	8.09691001300806	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs3130559	8E-9	8.09691001300806	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	0	0	0
rs2790216	8E-9	8.09691001300806	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs11168249	8E-9	8.09691001300806	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs17826255	8E-9	8.09691001300806	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs8090011	8E-9	8.09691001300806	22693455	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.	Type 2 diabetes	1	1	1	1
rs4841132	8E-9	8.09691001300806	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	0	0
rs7980687	8E-9	8.09691001300806	22504419	Common variants at 12q15 and 12q24 are associated with infant head circumference.	Head circumference (infant)	0	1	1	1
rs11229030	8E-9	8.09691001300806	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	1	1	1	1
rs10885997	8E-9	8.09691001300806	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs4650608	8E-9	8.09691001300806	22182935	Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.	Bipolar disorder	1	1	1	1
rs924043	8E-9	8.09691001300806	21980299	A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.	Type 1 diabetes	1	1	1	1
rs2798641	8E-9	8.09691001300806	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs4410871	8E-9	8.09691001300806	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs11057830	8E-9	8.09691001300806	21729881	Genome-wide association study identifies common variants associated with circulating vitamin E levels.	Vitamin E levels	0	1	1	1
rs2954026	8E-9	8.09691001300806	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	HDL Cholesterol - Triglycerides (HDLC-TG)	0	1	1	1
rs1387153	8E-9	8.09691001300806	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	0	0	0
rs514659	8E-9	8.09691001300806	21239051	Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies.	Coronary heart disease	0	0	1	1
rs10899489	8E-9	8.09691001300806	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	0	1	1	1
rs7562790	8E-9	8.09691001300806	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs1570106	8E-9	8.09691001300806	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs4759375	8E-9	8.09691001300806	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	1	1	1	1
rs17035378	8E-9	8.09691001300806	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs11712165	8E-9	8.09691001300806	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs2664170	8E-9	8.09691001300806	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	NA	NA	NA	NA
rs401681	8E-9	8.09691001300806	18978787	Common 5p15.33 and 6p21.33 variants influence lung cancer risk.	Lung cancer	0	0	1	1
rs4810485	8E-9	8.09691001300806	18794853	Common variants at CD40 and other loci confer risk of rheumatoid arthritis.	Rheumatoid arthritis	0	0	1	1
rs3848445	8E-9	8.09691001300806	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs2274432	8E-9	8.09691001300806	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs721048	8E-9	8.09691001300806	18264098	Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer.	Prostate cancer	1	1	1	1
rs7756992	8E-9	8.09691001300806	17460697	A variant in CDKAL1 influences insulin response and risk of type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs11951031	9E-9	8.04575749056067	23572186	Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearm.	Bone mineral density	1	1	1	1
rs6771725:rs10507246	9E-9	8.04575749056067	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs16865717:rs2009579	9E-9	8.04575749056067	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs2028385:rs2038227	9E-9	8.04575749056067	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs10476160:rs1707420	9E-9	8.04575749056067	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs971572:rs10828151	9E-9	8.04575749056067	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs2523608	9E-9	8.04575749056067	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	0	1	1	1
rs10091374	9E-9	8.04575749056067	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	1	1	1	1
rs399593	9E-9	8.04575749056067	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs72823592	9E-9	8.04575749056067	22949513	Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32	Epilepsy (generalized)	0	1	1	1
rs10496964	9E-9	8.04575749056067	22949513	Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32	Epilepsy (generalized)	1	1	1	1
rs16851720	9E-9	8.04575749056067	22841784	Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.	Hepatitis C induced liver fibrosis	1	1	1	1
rs1540283	9E-9	8.04575749056067	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	NA	NA	NA	NA
rs11223581	9E-9	8.04575749056067	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	1	1	1	1
rs8096445	9E-9	8.04575749056067	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune response to smallpox vaccine (IL-6)	1	1	1	1
rs10404486	9E-9	8.04575749056067	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs10757269	9E-9	8.04575749056067	22199011	Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.	Ankle-brachial index 	0	1	1	1
rs7694379	9E-9	8.04575749056067	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs17505102	9E-9	8.04575749056067	22076464	Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs16933812	9E-9	8.04575749056067	22013104	Genome-wide scan for loci of adolescent obesity and their relationship with blood pressure.	Obesity and blood pressure	1	1	1	1
rs932764	9E-9	8.04575749056067	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Hypertension	0	1	0	0
rs771767	9E-9	8.04575749056067	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs7238033	9E-9	8.04575749056067	21824976	A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3.	Bladder cancer	0	0	1	1
rs780094	9E-9	8.04575749056067	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	1	1
rs7130881	9E-9	8.04575749056067	21743057	Genome-wide association study identifies new prostate cancer susceptibility loci.	Prostate cancer	0	0	1	1
rs4711751	9E-9	8.04575749056067	21665990	Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs9349407	9E-9	8.04575749056067	21460841	Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.	Alzheimer's disease (late onset)	1	1	1	1
rs173539	9E-9	8.04575749056067	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome	0	0	0	0
rs2954033	9E-9	8.04575749056067	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Triglycerides-Blood Pressure (TG-BP)	0	1	0	0
rs420259	9E-9	8.04575749056067	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs1408272	9E-9	8.04575749056067	21149283	Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.	Iron status biomarkers	0	0	0	0
rs1998598	9E-9	8.04575749056067	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs736289	9E-9	8.04575749056067	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	1	1	1
rs2070776	9E-9	8.04575749056067	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	0	0	0
rs2652834	9E-9	8.04575749056067	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	1	1
rs10033900	9E-9	8.04575749056067	20385826	Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).	Age-related macular degeneration	0	0	1	1
rs17609240	9E-9	8.04575749056067	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Hematological parameters	0	1	1	1
rs884205	9E-9	8.04575749056067	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	0	1	1	1
rs8099917	9E-9	8.04575749056067	19749758	IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy.	Response to hepatitis C treatment	0	0	1	1
rs7826222	9E-9	8.04575749056067	19557161	Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.	Adiposity	NA	NA	NA	NA
rs742132	9E-9	8.04575749056067	19503597	Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.	Uric acid levels	0	1	1	1
rs766420	9E-9	8.04575749056067	19419973	Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.	Bilirubin levels	NA	NA	NA	NA
rs7422339	9E-9	8.04575749056067	20031577	Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.	Fibrinogen	NA	NA	NA	NA
rs10994336	9E-9	8.04575749056067	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	0	0	1	1
rs7524102	9E-9	8.04575749056067	18445777	Multiple genetic loci for bone mineral density and fractures.	Bone mineral density (spine)	0	0	0	0
rs1158167	9E-9	8.04575749056067	17903292	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.	Cystatin C	0	1	1	1
rs7591996	1E-8	8	23727862	Genome-wide association study identifies two susceptibility loci for osteosarcoma.	Osteosarcoma	1	1	1	1
rs17021463	1E-8	8	23666239	Meta-analysis identifies four new loci associated with testicular germ cell tumor.	Testicular germ cell tumor	1	1	1	1
rs10510452	1E-8	8	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	1	1	1	1
rs3134931	1E-8	8	23620142	Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.	Circulating myeloperoxidase levels (serum) 	NA	NA	NA	NA
rs4727443	1E-8	8	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	0	1	1	1
rs17083533	1E-8	8	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs7989336	1E-8	8	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	1	1	1	1
rs1514174	1E-8	8	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs2112347	1E-8	8	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	0	0	0
rs514716	1E-8	8	23562540	GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.	Alzheimer's disease biomarkers	0	0	0	0
rs10424878	1E-8	8	23555189	Genome-wide association study identifies genetic determinants of urine PCA3 levels in men.	PCA3 expression level	0	1	1	1
rs6678914	1E-8	8	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	1	1	1	1
rs616488	1E-8	8	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	0	0	1	1
rs2016394	1E-8	8	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs10759243	1E-8	8	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs10032549	1E-8	8	23535967	Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate.	Glomerular filtration rate	0	0	0	0
rs17631303	1E-8	8	23544013	Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.	Ovarian cancer in BRCA1 mutation carriers 	0	1	1	1
rs6738962	1E-8	8	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs4700060	1E-8	8	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs148763909	1E-8	8	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs11154851	1E-8	8	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs6858430:rs4800250	1E-8	8	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs467650:rs7153749	1E-8	8	23509962	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.	Venous thromboembolism (gene x gene interaction)	NA	NA	NA	NA
rs1172294	1E-8	8	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs11191454	1E-8	8	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	0	0	0
rs11191580	1E-8	8	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	0	0	0
rs16899524	1E-8	8	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	0	1	1	1
rs9307551	1E-8	8	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs1254319	1E-8	8	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	0	1	1	1
rs1537424	1E-8	8	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs10799824	1E-8	8	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs4930561	1E-8	8	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11710456	1E-8	8	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6583437	1E-8	8	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2072209	1E-8	8	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4917017	1E-8	8	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6421315	1E-8	8	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7620503	1E-8	8	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs2079742	1E-8	8	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs17786744	1E-8	8	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs11654749	1E-8	8	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs477692	1E-8	8	23047291	A genome-wide association analysis of temozolomide response using lymphoblastoid cell lines shows a clinically relevant association with MGMT.	Response to temozolomide	1	1	1	1
rs7015630	1E-8	8	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs2930047	1E-8	8	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs38904	1E-8	8	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs11612508	1E-8	8	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs9847710	1E-8	8	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	0	1	1	1
rs483905	1E-8	8	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	1	1	1	1
rs11672691	1E-8	8	23065704	A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease.	Prostate cancer	0	0	0	0
rs9268516	1E-8	8	23028483	Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA.	Asthma	0	1	1	1
rs694419	1E-8	8	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	0	0	0	0
rs3777200	1E-8	8	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum total protein level	0	1	1	1
rs412658	1E-8	8	23001564	Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans.	Telomere length	1	1	1	1
rs1317082	1E-8	8	23001564	Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans.	Telomere length	0	0	1	1
rs7583877	1E-8	8	23028342	New susceptibility loci associated with kidney disease in type 1 diabetes.	Type 1 diabetes nephropathy	1	1	1	1
rs2284378	1E-8	8	22976474	A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.	Breast cancer	0	1	1	1
rs17065417	1E-8	8	22941191	Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.	Neuroblastoma	0	0	0	0
rs10822184	1E-8	8	22936694	Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men.	Androgen levels	0	1	1	1
rs4977756	1E-8	8	22886559	Genome-wide association study of glioma and meta-analysis.	Glioma	0	0	1	1
rs7590268	1E-8	8	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs12371778	1E-8	8	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	0	1	1	1
rs7178572	1E-8	8	22693455	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.	Type 2 diabetes	1	1	1	1
rs17007761	1E-8	8	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs7105056	1E-8	8	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-12p40)	1	1	1	1
rs7658486	1E-8	8	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-12p40)	1	1	1	1
rs2268118	1E-8	8	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	1	1	1	1
rs4794820	1E-8	8	22561531	Genome-wide association study to identify genetic determinants of severe asthma.	Asthma	0	0	1	1
rs11656696	1E-8	8	22570627	Common genetic determinants of intraocular pressure and primary open-angle glaucoma.	Intraocular pressure	1	1	1	1
rs1265507	1E-8	8	22532574	Identification of a novel percent mammographic density locus at 12q24.	Mammographic density	1	1	1	1
rs2517532	1E-8	8	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	0	1	1	1
rs157582	1E-8	8	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs11662721	1E-8	8	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs17718828	1E-8	8	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs870288	1E-8	8	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs1566039	1E-8	8	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Sphingolipid levels	1	1	1	1
rs20541	1E-8	8	22286212	Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups.	Hodgkin's lymphoma	0	1	1	1
rs13017599	1E-8	8	22170493	Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL.	Psoriatic arthritis	0	1	1	1
rs2336384	1E-8	8	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	0	1	1	1
rs17824620	1E-8	8	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs2300290	1E-8	8	22126837	Genome-wide study identifies PTPRO and WDR72 and FOXQ1-SUMO1P1 interaction associated with neurocognitive function.	Cognitive function	1	1	1	1
rs2858331	1E-8	8	22075330	A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study.	IgE levels 	0	1	1	1
rs2155219	1E-8	8	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	IgE grass sensitization	0	1	1	1
rs17513503	1E-8	8	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	IgE grass sensitization	1	1	1	1
rs1789891	1E-8	8	22004471	Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.	Alcohol dependence	1	1	1	1
rs993925	1E-8	8	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs11172113	1E-8	8	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	1	1	1
rs871606	1E-8	8	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	1	1	1	1
rs10466829	1E-8	8	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs13333054	1E-8	8	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	0	1	1
rs17174870	1E-8	8	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs874628	1E-8	8	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs13192841	1E-8	8	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs4788084	1E-8	8	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	1	1	1
rs4906844	1E-8	8	21810643	Association of genetic variants on 15q12 with cortical thickness and cognition in schizophrenia.	Cortical thickness	1	1	1	1
rs1692120	1E-8	8	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs9296015	1E-8	8	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	1	1	1
rs5919432	1E-8	8	21743467	Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.	Prostate cancer	NA	NA	NA	NA
rs6547705	1E-8	8	21685912	Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.	Progressive supranuclear palsy	1	1	1	1
rs1999930	1E-8	8	21665990	Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.	Age-related macular degeneration	0	1	1	1
rs1494961	1E-8	8	21437268	A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium.	Upper aerodigestive tract cancers	0	1	1	1
rs439401	1E-8	8	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	HDL Cholesterol - Triglycerides (HDLC-TG)	0	1	1	1
rs9987289	1E-8	8	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	HDL Cholesterol - Triglycerides (HDLC-TG)	0	1	1	1
rs2043085	1E-8	8	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	1	1	1
rs12286037	1E-8	8	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	0	0	0
rs17609940	1E-8	8	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	1	1	1
rs17465637	1E-8	8	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	1	1	1
rs9846232	1E-8	8	21368711	Genome-wide association study of personality traits in bipolar patients.	Personality dimensions	1	1	1	1
rs11203203	1E-8	8	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	0	1	1	1
rs7579944	1E-8	8	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	1	1	1	1
rs4705952	1E-8	8	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	0	1	1	1
rs6911490	1E-8	8	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs9378249	1E-8	8	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	0	1	1	1
rs10483776	1E-8	8	21203500	Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation.	N-glycan levels	0	0	0	0
rs6575793	1E-8	8	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs4929923	1E-8	8	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	0	1	1	1
rs6439371	1E-8	8	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs1456896	1E-8	8	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs6908425	1E-8	8	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs9912468	1E-8	8	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs1886512	1E-8	8	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs2242285	1E-8	8	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs2981575	1E-8	8	21060860	Common genetic variants and modification of penetrance of BRCA2-associated breast cancer.	Breast cancer	0	0	1	1
rs1997111	1E-8	8	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	T-tau	1	1	1	1
rs12694997	1E-8	8	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs6569992	1E-8	8	20927387	A genome-wide association study of red blood cell traits using the electronic medical record.	Red blood cell traits	0	0	0	0
rs2230199	1E-8	8	20861866	Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs2284033	1E-8	8	20860503	A large-scale, consortium-based genomewide association study of asthma.	Asthma	1	1	1	1
rs6474359	1E-8	8	20858683	Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.	Glycated hemoglobin levels	1	1	1	1
rs2755237	1E-8	8	20719862	New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.	Central corneal thickness	0	0	1	1
rs6496932	1E-8	8	20719862	New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.	Central corneal thickness	0	1	1	1
rs448378	1E-8	8	20700443	Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.	Magnesium levels	0	1	1	1
rs7206971	1E-8	8	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs7570971	1E-8	8	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	1	1
rs181362	1E-8	8	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	1	1
rs2902940	1E-8	8	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	LDL cholesterol	0	1	0	0
rs4765127	1E-8	8	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	0	0
rs11776767	1E-8	8	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	1	1	1	1
rs3802177	1E-8	8	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	0	1	1	1
rs1547014	1E-8	8	20548946	A genome-wide association study of optic disc parameters.	Vertical cup-disc ratio	1	1	1	1
rs1926320	1E-8	8	20548946	A genome-wide association study of optic disc parameters.	Vertical cup-disc ratio	1	1	1	1
rs3087243	1E-8	8	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	0	1	1
rs10519210	1E-8	8	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	1	1	1	1
rs10846744	1E-8	8	20442857	Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study.	Lipoprotein-associated phospholipase A2 activity and mass	0	0	1	1
rs3733829	1E-8	8	20418890	Genome-wide meta-analyses identify multiple loci associated with smoking behavior.	Smoking behavior	0	1	1	1
rs6474412	1E-8	8	20418888	Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior.	Smoking behavior	1	1	1	1
rs10468017	1E-8	8	20385826	Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).	Age-related macular degeneration	0	0	1	1
rs10794720	1E-8	8	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs10109414	1E-8	8	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	0	1	1	1
rs3024505	1E-8	8	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	0	0	1	1
rs11190140	1E-8	8	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	0	0	1	1
rs1834481	1E-8	8	20150558	Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels.	Interleukin-18 levels	0	0	0	0
rs4506565	1E-8	8	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	1	1	1
rs227731	1E-8	8	20023658	Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.	Orofacial clefts	0	1	1	1
rs9303521	1E-8	8	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	0	1	1	1
rs2016266	1E-8	8	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	1	1	1	1
rs4689388	1E-8	8	19734900	Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia.	Type 2 diabetes and other traits	1	1	1	1
rs3849942	1E-8	8	19734901	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	0	0	0	0
rs498872	1E-8	8	19578367	Genome-wide association study identifies five susceptibility loci for glioma.	Glioma	0	0	1	1
rs13194053	1E-8	8	19571811	Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.	Schizophrenia	0	0	1	1
rs7590720	1E-8	8	19581569	Genome-wide association study of alcohol dependence.	Alcohol dependence	1	1	1	1
rs12356193	1E-8	8	19503597	Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.	Uric acid levels	0	1	1	1
rs10937275	1E-8	8	19483685	HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin.	Drug-induced liver injury (flucloxacillin)	1	1	1	1
rs11014166	1E-8	8	19430479	Genome-wide association study of blood pressure and hypertension.	Diastolic blood pressure	0	1	1	1
rs12946454	1E-8	8	19430483	Genome-wide association study identifies eight loci associated with blood pressure.	Systolic blood pressure	0	1	1	1
rs2282978	1E-8	8	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs1539019	1E-8	8	20031576	Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts.	Fibrinogen	0	1	1	1
rs6725887	1E-8	8	19198609	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.	Myocardial infarction (early onset)	0	1	1	1
rs11206510	1E-8	8	19198609	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.	Myocardial infarction (early onset)	0	1	1	1
rs10889677	1E-8	8	19122664	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.	Ulcerative colitis	0	0	1	1
rs11209026	1E-8	8	19122664	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.	Ulcerative colitis	0	0	1	1
rs13194491	1E-8	8	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	1	1	1	1
rs10913469	1E-8	8	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	1	1	1
rs2967605	1E-8	8	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	HDL cholesterol	1	1	1	1
rs9929218	1E-8	8	19011631	Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer.	Colorectal cancer	1	1	1	1
rs864643	1E-8	8	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs7995215	1E-8	8	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs8034191	1E-8	8	18780872	Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer.	Lung cancer	0	0	1	1
rs477515	1E-8	8	18758464	Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs2476601	1E-8	8	18587394	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.	Crohn's disease	0	0	1	1
rs1776897	1E-8	8	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs2282978	1E-8	8	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs314277	1E-8	8	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	0	0	1	1
rs4607103	1E-8	8	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	0	1	1	1
rs495337	1E-8	8	18364390	Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene.	Psoriasis	1	1	1	1
rs10496265	1E-8	8	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Aging traits	1	1	1	1
rs763361	1E-8	8	17554260	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs7903146	1E-8	8	17463248	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.	Type 2 diabetes	0	0	1	1
rs10946398	1E-8	8	17463249	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs10012307	2E-8	7.69897000433602	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (parent-of-origin)	1	1	1	1
rs1056667	2E-8	7.69897000433602	23722424	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.	Educational attainment	1	1	1	1
rs7924176	2E-8	7.69897000433602	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (time to first tooth eruption)	0	1	0	0
rs3790672	2E-8	7.69897000433602	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	1	1	1	1
rs3805663	2E-8	7.69897000433602	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	0	1	1	1
rs368433	2E-8	7.69897000433602	23652523	Identification of genetic loci associated with Helicobacter pylori serologic status.	Helicobacter pylori serologic status	0	1	1	1
rs11191865	2E-8	7.69897000433602	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	1	1	1	1
rs9285425	2E-8	7.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs6750795	2E-8	7.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs6855629	2E-8	7.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs17511102	2E-8	7.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs13041126	2E-8	7.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	1	1	1	1
rs7503807	2E-8	7.69897000433602	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	1	1	1	1
rs3101336	2E-8	7.69897000433602	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	0	0	0	0
rs1218582	2E-8	7.69897000433602	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	0	1	1	1
rs11552449	2E-8	7.69897000433602	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	0	1	1	1
rs12493607	2E-8	7.69897000433602	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs11199914	2E-8	7.69897000433602	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	0	1	1	1
rs1243180	2E-8	7.69897000433602	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	0	1	1	1
rs1126809	2E-8	7.69897000433602	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Sunburns	NA	NA	NA	NA
rs17393344	2E-8	7.69897000433602	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs115102486	2E-8	7.69897000433602	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs3812111	2E-8	7.69897000433602	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs9542236	2E-8	7.69897000433602	23455636	Seven new loci associated with age-related macular degeneration.	Age-related macular degeneration	1	1	1	1
rs2377339	2E-8	7.69897000433602	23533358	NCK2 is significantly associated with opiates addiction in African-origin men.	Addiction	0	0	0	0
rs14165	2E-8	7.69897000433602	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs2184971	2E-8	7.69897000433602	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs235770	2E-8	7.69897000433602	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs9497965	2E-8	7.69897000433602	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs7825175	2E-8	7.69897000433602	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs7860634	2E-8	7.69897000433602	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs17651119	2E-8	7.69897000433602	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs1049110	2E-8	7.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs2186369	2E-8	7.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4530903	2E-8	7.69897000433602	23349640	Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.	Lymphoma	0	0	0	0
rs2307394	2E-8	7.69897000433602	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs2865531	2E-8	7.69897000433602	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs322458	2E-8	7.69897000433602	23223146	A genome-wide association study in Caucasian women points out a putative role of the STXBP5L gene in facial photoaging.	Aging (facial)	1	1	1	1
rs2075650	2E-8	7.69897000433602	23207651	A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing.	Cognitive decline	0	0	1	1
rs9272346	2E-8	7.69897000433602	23181788	HLA-DQ strikes again: genome-wide association study further confirms HLA-DQ in the diagnosis of asthma among adults.	Asthma	0	0	1	1
rs12105918	2E-8	7.69897000433602	23184150	Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer.	Renal cell carcinoma	1	1	1	1
rs6837335	2E-8	7.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	1	1	1	1
rs2651244	2E-8	7.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs6740462	2E-8	7.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs2111485	2E-8	7.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs12654812	2E-8	7.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs12199775	2E-8	7.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs6592362	2E-8	7.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs11739663	2E-8	7.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	0	0	1	1
rs4722672	2E-8	7.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	1	1	1	1
rs28374715	2E-8	7.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	1	1	1	1
rs6088765	2E-8	7.69897000433602	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	0	1	1	1
rs3896439	2E-8	7.69897000433602	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs665440	2E-8	7.69897000433602	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	NA	NA	NA	NA
rs879324	2E-8	7.69897000433602	23041239	Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.	Stroke (ischemic)	0	1	1	1
rs1260326	2E-8	7.69897000433602	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	0	0	0	0
rs16948098	2E-8	7.69897000433602	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	0	1	1	1
rs3027234	2E-8	7.69897000433602	23001564	Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans.	Telomere length	1	1	1	1
rs17036170	2E-8	7.69897000433602	22968431	Limited contribution of common genetic variants to risk for liver injury due to a variety of drugs.	Drug-induced liver injury 	1	1	1	1
rs5934505	2E-8	7.69897000433602	22936694	Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men.	Androgen levels	NA	NA	NA	NA
rs227731	2E-8	7.69897000433602	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	0	0	1	1
rs12543318	2E-8	7.69897000433602	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs4149056	2E-8	7.69897000433602	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	1	1	1
rs5904818	2E-8	7.69897000433602	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	NA	NA	NA	NA
rs9332739	2E-8	7.69897000433602	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (CNV)	0	0	0	0
rs4713226	2E-8	7.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	0	1	1	1
rs17231212	2E-8	7.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-10)	1	1	1	1
rs16948200	2E-8	7.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	1	1	1	1
rs1403155	2E-8	7.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	1	1	1	1
rs4251424	2E-8	7.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted TNF-alpha)	NA	NA	NA	NA
rs17444059	2E-8	7.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune response to smallpox vaccine (IL-6)	1	1	1	1
rs17817600	2E-8	7.69897000433602	22832961	Genome-wide association study of Alzheimer's disease.	Alzheimer's disease	0	0	1	1
rs9315702	2E-8	7.69897000433602	22745009	Multiple loci influencing hippocampal degeneration identified by genome scan.	Hippocampal atrophy	1	1	1	1
rs1483121	2E-8	7.69897000433602	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	1	1	1	1
rs2785980	2E-8	7.69897000433602	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	0	1	1	1
rs1659258	2E-8	7.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs16872571	2E-8	7.69897000433602	22561518	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.	Vitiligo	0	1	1	1
rs853308	2E-8	7.69897000433602	22561518	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.	Vitiligo	1	1	1	1
rs7555523	2E-8	7.69897000433602	22570627	Common genetic determinants of intraocular pressure and primary open-angle glaucoma.	Intraocular pressure	0	1	1	1
rs9815663	2E-8	7.69897000433602	22560479	Genome-wide association study of the age of onset of childhood asthma.	Asthma (childhood onset)	1	1	1	1
rs10917477	2E-8	7.69897000433602	22494929	Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function.	Thyroid function	0	1	1	1
rs925735	2E-8	7.69897000433602	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	1	1	1
rs4805885	2E-8	7.69897000433602	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	0	0	0
rs7705924	2E-8	7.69897000433602	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	1	1	1	1
rs12677663	2E-8	7.69897000433602	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	1	1	1	1
rs3099844	2E-8	7.69897000433602	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs1985671	2E-8	7.69897000433602	22365631	Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.	Temperament (bipolar disorder)	1	1	1	1
rs17018311	2E-8	7.69897000433602	22365631	Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.	Temperament (bipolar disorder)	1	1	1	1
rs12472274	2E-8	7.69897000433602	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs197770	2E-8	7.69897000433602	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs2945816	2E-8	7.69897000433602	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	NA	NA	NA	NA
rs7337573	2E-8	7.69897000433602	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	NA	NA	NA	NA
rs4485401	2E-8	7.69897000433602	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Sphingolipid levels	1	1	1	1
rs1039002	2E-8	7.69897000433602	22205951	Genome-wide association study in bipolar patients stratified by co-morbidity.	Bipolar disorder	1	1	1	1
rs170934	2E-8	7.69897000433602	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs708382	2E-8	7.69897000433602	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs4921542	2E-8	7.69897000433602	22137330	Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.	Creutzfeldt-Jakob disease (variant)	1	1	1	1
rs1052501	2E-8	7.69897000433602	22120009	Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.	Multiple myeloma	0	1	1	1
rs17505102	2E-8	7.69897000433602	22076464	Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	0	0	0	0
rs340005	2E-8	7.69897000433602	22010049	Loci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations.	Gamma gluatamyl transferase levels	0	1	1	1
rs153916	2E-8	7.69897000433602	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs1260326	2E-8	7.69897000433602	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	1	1	1
rs7914558	2E-8	7.69897000433602	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	0	1	1
rs10503253	2E-8	7.69897000433602	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	1	1	1	1
rs4765913	2E-8	7.69897000433602	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	0	1	1	1
rs445925	2E-8	7.69897000433602	21909108	Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.	Carotid intima media thickness	0	1	1	1
rs6601530	2E-8	7.69897000433602	21909108	Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.	Carotid intima media thickness	0	1	1	1
rs1327235	2E-8	7.69897000433602	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	0	1	0	0
rs13002573	2E-8	7.69897000433602	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	0	0	0
rs4129267	2E-8	7.69897000433602	21907864	Identification of IL6R and chromosome 11q13.5 as risk loci for asthma.	Asthma	0	1	1	1
rs7130588	2E-8	7.69897000433602	21907864	Identification of IL6R and chromosome 11q13.5 as risk loci for asthma.	Asthma	0	1	1	1
rs11842874	2E-8	7.69897000433602	21871595	A variant in MCF2L is associated with osteoarthritis.	Osteoarthritis	1	1	1	1
rs2300603	2E-8	7.69897000433602	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs6897932	2E-8	7.69897000433602	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs140522	2E-8	7.69897000433602	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs1323292	2E-8	7.69897000433602	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs4285028	2E-8	7.69897000433602	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs3130501	2E-8	7.69897000433602	21801394	Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.	Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS-TEN)	0	1	1	1
rs11230874	2E-8	7.69897000433602	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs4779584	2E-8	7.69897000433602	21761138	Meta-analysis of new genome-wide association studies of colorectal cancer risk.	Colorectal cancer	1	1	1	1
rs6556416	2E-8	7.69897000433602	21743469	Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.	Ankylosing spondylitis	0	1	1	1
rs6763931	2E-8	7.69897000433602	21743467	Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.	Prostate cancer	0	1	1	1
rs597503	2E-8	7.69897000433602	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs17718586	2E-8	7.69897000433602	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	0	1	1	1
rs2185570	2E-8	7.69897000433602	21533175	Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.	Dehydroepiandrosterone sulphate levels	0	1	1	1
rs6738028	2E-8	7.69897000433602	21533175	Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.	Dehydroepiandrosterone sulphate levels	1	1	1	1
rs4767364	2E-8	7.69897000433602	21437268	A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium.	Upper aerodigestive tract cancers	0	1	1	1
rs1372072	2E-8	7.69897000433602	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	1	1	1	1
rs46522	2E-8	7.69897000433602	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	1	1	1
rs975730	2E-8	7.69897000433602	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	1	1	1	1
rs1876518	2E-8	7.69897000433602	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	0	1	1	1
rs2847281	2E-8	7.69897000433602	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	0	1	1	1
rs4728142	2E-8	7.69897000433602	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	0	1	1
rs1320448	2E-8	7.69897000433602	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	1	1	1	1
rs4973768	2E-8	7.69897000433602	21263130	Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study.	Breast cancer	0	0	1	1
rs7953249	2E-8	7.69897000433602	21203500	Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation.	N-glycan levels	0	1	1	1
rs900145	2E-8	7.69897000433602	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	0	1	1	1
rs6762477	2E-8	7.69897000433602	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	0	1	1	1
rs2947411	2E-8	7.69897000433602	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	0	1	1	1
rs1361108	2E-8	7.69897000433602	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	0	1	1	1
rs1364063	2E-8	7.69897000433602	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	0	1	1	1
rs633715	2E-8	7.69897000433602	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	0	1	1	1
rs4840086	2E-8	7.69897000433602	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs4074536	2E-8	7.69897000433602	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs11855415	2E-8	7.69897000433602	21051773	PCSK6 is associated with handedness in individuals with dyslexia.	Handedness in dyslexia	1	1	1	1
rs1432295	2E-8	7.69897000433602	21037568	A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).	Hodgkin's lymphoma	0	1	1	1
rs12586317	2E-8	7.69897000433602	20953189	Genome-wide association analysis identifies three psoriasis susceptibility loci.	Psoriasis	0	0	1	1
rs494459	2E-8	7.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs425277	2E-8	7.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs7864648	2E-8	7.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1814175	2E-8	7.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs4640244	2E-8	7.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1401796	2E-8	7.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	NA	NA	NA	NA
rs2142672	2E-8	7.69897000433602	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	LDL cholesterol	0	0	1	1
rs2737229	2E-8	7.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs1800562	2E-8	7.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	0	0
rs11613352	2E-8	7.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	0	0
rs2412710	2E-8	7.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	1	1	1	1
rs2972146	2E-8	7.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	0	0
rs2068888	2E-8	7.69897000433602	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	1	1	1	1
rs12666989	2E-8	7.69897000433602	20639392	Genome-wide association analysis identifies multiple loci related to resting heart rate.	Resting heart rate	0	0	0	0
rs2383207	2E-8	7.69897000433602	20622881	Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.	Abdominal aortic aneurysm	0	1	1	1
rs7957197	2E-8	7.69897000433602	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	0	1	1	1
rs504963	2E-8	7.69897000433602	20570966	Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.	Crohn's disease	0	0	1	1
rs1900004	2E-8	7.69897000433602	20548946	A genome-wide association study of optic disc parameters.	Vertical cup-disc ratio	0	1	0	0
rs6265	2E-8	7.69897000433602	20418890	Genome-wide meta-analyses identify multiple loci associated with smoking behavior.	Smoking behavior	0	1	1	1
rs9380272	2E-8	7.69897000433602	20385819	Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.	Age-related macular degeneration	NA	NA	NA	NA
rs493258	2E-8	7.69897000433602	20385826	Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).	Age-related macular degeneration	0	0	0	0
rs2230199	2E-8	7.69897000433602	20385826	Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).	Age-related macular degeneration	0	0	1	1
rs8014194	2E-8	7.69897000433602	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs371915	2E-8	7.69897000433602	20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Eosinophilic esophagitis (pediatric)	1	1	1	1
rs9674544	2E-8	7.69897000433602	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (number of teeth)	0	0	1	1
rs13180	2E-8	7.69897000433602	20173748	Variants in FAM13A are associated with chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease	0	0	1	1
rs7758512	2E-8	7.69897000433602	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	0	1	1	1
rs7078160	2E-8	7.69897000433602	20023658	Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.	Orofacial clefts	0	0	1	1
rs4299376	2E-8	7.69897000433602	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	1	1	1
rs4939883	2E-8	7.69897000433602	19936222	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Lipid metabolism phenotypes	0	0	0	0
rs10788819	2E-8	7.69897000433602	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	0	0	0	0
rs4324798	2E-8	7.69897000433602	19836008	A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.	Lung adenocarcinoma	0	1	1	1
rs1800562	2E-8	7.69897000433602	19820699	Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.	Iron status biomarkers	0	0	1	1
rs11071720	2E-8	7.69897000433602	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	0	1	1	1
rs228769	2E-8	7.69897000433602	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (hip)	1	1	1	1
rs10048146	2E-8	7.69897000433602	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	1	1	1	1
rs11898505	2E-8	7.69897000433602	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	1	1	1	1
rs1471403	2E-8	7.69897000433602	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	1	1	1	1
rs1465618	2E-8	7.69897000433602	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	0	1	1	1
rs6465657	2E-8	7.69897000433602	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	0	0	1	1
rs10986018	2E-8	7.69897000433602	19744961	Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.	Folate pathway vitamin levels	1	1	1	1
rs10770612	2E-8	7.69897000433602	19584346	Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.	Aortic root size	1	1	1	1
rs1541160	2E-8	7.69897000433602	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs710841	2E-8	7.69897000433602	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs13387042	2E-8	7.69897000433602	19330030	A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).	Breast cancer	0	0	1	1
rs11864477	2E-8	7.69897000433602	19249006	Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groups.	Bone mineral density	1	1	1	1
rs3914132	2E-8	7.69897000433602	19230858	A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.	Otosclerosis	1	1	1	1
rs1513670	2E-8	7.69897000433602	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (hip)	1	1	1	1
rs6696981	2E-8	7.69897000433602	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (spine)	0	0	0	0
rs2568958	2E-8	7.69897000433602	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	1	0	0
rs2844479	2E-8	7.69897000433602	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	1	1	1
rs11084753	2E-8	7.69897000433602	19079261	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.	Body mass index	0	0	1	1
rs2650000	2E-8	7.69897000433602	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	LDL cholesterol	0	0	1	1
rs10401969	2E-8	7.69897000433602	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	LDL cholesterol	0	0	0	0
rs673548	2E-8	7.69897000433602	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	Metabolic traits	0	1	0	0
rs229541	2E-8	7.69897000433602	18978792	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.	Type 1 diabetes	0	1	1	1
rs11597390	2E-8	7.69897000433602	18940312	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.	Liver enzyme levels	0	1	1	1
rs9976767	2E-8	7.69897000433602	18840781	Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.	Type 1 diabetes	0	0	1	1
rs2618476	2E-8	7.69897000433602	19165918	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.	Systemic lupus erythematosus	0	0	1	1
rs9594738	2E-8	7.69897000433602	18445777	Multiple genetic loci for bone mineral density and fractures.	Bone mineral density (hip)	0	1	0	0
rs1999805	2E-8	7.69897000433602	18445777	Multiple genetic loci for bone mineral density and fractures.	Bone mineral density (spine)	0	0	1	1
rs1169310	2E-8	7.69897000433602	18439552	Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein.	C-reactive protein	0	0	1	1
rs8192284	2E-8	7.69897000433602	18439548	Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.	C-reactive protein	NA	NA	NA	NA
rs4743034	2E-8	7.69897000433602	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs967417	2E-8	7.69897000433602	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs6686842	2E-8	7.69897000433602	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs10906982	2E-8	7.69897000433602	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs6724465	2E-8	7.69897000433602	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs12130333	2E-8	7.69897000433602	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	Triglycerides	0	0	1	1
rs4775041	2E-8	7.69897000433602	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	Triglycerides	0	0	0	0
rs2722425	2E-8	7.69897000433602	17903298	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	Fasting plasma glucose	1	1	1	1
rs1012053	2E-8	7.69897000433602	17486107	A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder.	Bipolar disorder	1	1	1	1
rs11933531	3E-8	7.52287874528034	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	1	1	1	1
rs11687170	3E-8	7.52287874528034	23722424	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.	Educational attainment	0	0	0	0
rs10932688	3E-8	7.52287874528034	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (number of teeth)	0	1	1	1
rs9316505	3E-8	7.52287874528034	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (number of teeth)	1	1	1	1
rs997154	3E-8	7.52287874528034	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (number of teeth)	1	1	1	1
rs2072499	3E-8	7.52287874528034	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	1	1	1	1
rs7552186	3E-8	7.52287874528034	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs3103267	3E-8	7.52287874528034	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	0	0	1	1
rs17381664	3E-8	7.52287874528034	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	1	1	1	1
rs10968576	3E-8	7.52287874528034	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	0	1	1	1
rs13389219	3E-8	7.52287874528034	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Waist-hip ratio	0	0	1	1
rs11902236	3E-8	7.52287874528034	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs10472076	3E-8	7.52287874528034	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs7904519	3E-8	7.52287874528034	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	0	1	1	1
rs1550623	3E-8	7.52287874528034	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs1353747	3E-8	7.52287874528034	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs1436904	3E-8	7.52287874528034	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs183211	3E-8	7.52287874528034	23544013	Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.	Ovarian cancer in BRCA1 mutation carriers 	0	1	1	1
rs4691139	3E-8	7.52287874528034	23544013	Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.	Ovarian cancer in BRCA1 mutation carriers 	1	1	1	1
rs34972666	3E-8	7.52287874528034	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs1864729	3E-8	7.52287874528034	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs7004633	3E-8	7.52287874528034	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs4478858	3E-8	7.52287874528034	23455491	NKAIN1-SERINC2 is a functional, replicable and genome-wide significant risk gene region specific for alcohol dependence in subjects of European descent.	Alcohol dependence	1	1	1	1
rs509208	3E-8	7.52287874528034	23419831	APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.	Alzheimer's disease biomarkers	1	1	1	1
rs3184504	3E-8	7.52287874528034	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	0	1	1	1
rs4793501	3E-8	7.52287874528034	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs1571583	3E-8	7.52287874528034	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	1	1	1
rs9497965	3E-8	7.52287874528034	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs7240777	3E-8	7.52287874528034	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs12054895	3E-8	7.52287874528034	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs909674	3E-8	7.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2186369	3E-8	7.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7224668	3E-8	7.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6583437	3E-8	7.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11847263	3E-8	7.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7953704	3E-8	7.52287874528034	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs12530845	3E-8	7.52287874528034	23222517	Seventy-five genetic loci influencing the human red blood cell.	Red blood cell traits	1	1	1	1
rs10486483	3E-8	7.52287874528034	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Crohn's disease	0	1	1	1
rs2472649	3E-8	7.52287874528034	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs7911264	3E-8	7.52287874528034	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	0	1	1	1
rs4899554	3E-8	7.52287874528034	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs1016883	3E-8	7.52287874528034	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	0	1	1	1
rs2187689	3E-8	7.52287874528034	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs926849	3E-8	7.52287874528034	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs4820425	3E-8	7.52287874528034	22936669	A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.	Crohn's disease	0	1	1	1
rs7868992	3E-8	7.52287874528034	22889924	Genome-wide association study of Tourette's syndrome.	Tourette syndrome	1	1	1	1
rs1452787	3E-8	7.52287874528034	22821403	Genome-wide association analysis in Primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4.	Sclerosing cholangitis and ulcerative colitis (combined)	0	1	1	1
rs3779195	3E-8	7.52287874528034	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	1	1	1
rs293428	3E-8	7.52287874528034	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	1	1	1	1
rs17135437	3E-8	7.52287874528034	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	NA	NA	NA	NA
rs9349379	3E-8	7.52287874528034	22683712	Genome-wide association analysis identifies susceptibility loci for migraine without aura.	Migraine	0	1	1	1
rs11172113	3E-8	7.52287874528034	22683712	Genome-wide association analysis identifies susceptibility loci for migraine without aura.	Migraine	0	0	1	1
rs10195263	3E-8	7.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs11564024	3E-8	7.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-1beta)	NA	NA	NA	NA
rs9582259	3E-8	7.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-1beta)	1	1	1	1
rs3757247	3E-8	7.52287874528034	22561518	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.	Vitiligo	0	1	1	1
rs998584	3E-8	7.52287874528034	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	1	1	1
rs10734105	3E-8	7.52287874528034	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	1	1	1	1
rs10769780	3E-8	7.52287874528034	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs12423247	3E-8	7.52287874528034	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs9932186	3E-8	7.52287874528034	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs7018475	3E-8	7.52287874528034	22293688	1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.	Type 2 diabetes	0	0	1	1
rs2727943	3E-8	7.52287874528034	22205951	Genome-wide association study in bipolar patients stratified by co-morbidity.	Bipolar disorder	1	1	1	1
rs763780	3E-8	7.52287874528034	22142827	A genome-wide association study of overall survival in pancreatic cancer patients treated with gemcitabine in CALGB 80303.	Response to gemcitabine in pancreatic cancer 	1	1	1	1
rs2150702	3E-8	7.52287874528034	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	1	1	1	1
rs6718520	3E-8	7.52287874528034	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs17396340	3E-8	7.52287874528034	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	0	1	1	1
rs7149242	3E-8	7.52287874528034	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs1034566	3E-8	7.52287874528034	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs1945213	3E-8	7.52287874528034	22076464	Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs247616	3E-8	7.52287874528034	22003152	Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies.	Lipoprotein-associated phospholipase A2 activity and mass	0	0	1	1
rs401681	3E-8	7.52287874528034	21983787	Genome-wide association study identifies three new melanoma susceptibility loci.	Melanoma	0	1	1	1
rs9978142	3E-8	7.52287874528034	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	1	1	1
rs1344555	3E-8	7.52287874528034	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs11191580	3E-8	7.52287874528034	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	0	0	0
rs12966547	3E-8	7.52287874528034	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	1	1	1
rs734597	3E-8	7.52287874528034	21935397	Genome-wide population-based association study of extremely overweight young adults--the GOYA study.	Obesity (extreme)	0	1	1	1
rs2521501	3E-8	7.52287874528034	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs319690	3E-8	7.52287874528034	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	1	1	1	1
rs381815	3E-8	7.52287874528034	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs11755527	3E-8	7.52287874528034	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	1	1	1
rs6918936	3E-8	7.52287874528034	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	0	0
rs130067	3E-8	7.52287874528034	21743467	Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.	Prostate cancer	0	1	1	1
rs4730775	3E-8	7.52287874528034	21732829	Wnt signaling and Dupuytren's disease.	Dupuytren's disease	0	1	1	1
rs7335046	3E-8	7.52287874528034	21700618	Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma.	Basal cell carcinoma 	0	1	1	1
rs11624056	3E-8	7.52287874528034	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs13204965	3E-8	7.52287874528034	21533022	Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.	Bone mineral density	0	1	1	1
rs4961252	3E-8	7.52287874528034	21502966	Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients.	Response to interferon beta therapy	1	1	1	1
rs1800562	3E-8	7.52287874528034	21483845	Genome-wide association study identifies genetic loci associated with iron deficiency.	Iron status biomarkers	0	0	0	0
rs1441756	3E-8	7.52287874528034	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	0	0	0
rs2306374	3E-8	7.52287874528034	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	0	1	1
rs11739663	3E-8	7.52287874528034	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	0	1	1
rs4765623	3E-8	7.52287874528034	21131975	Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3.	Renal cell carcinoma	1	1	1	1
rs1925690	3E-8	7.52287874528034	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	MRI atrophy measures	1	1	1	1
rs8093763	3E-8	7.52287874528034	21106707	A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity.	Bleomycin sensitivity	1	1	1	1
rs7617480	3E-8	7.52287874528034	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs9939609	3E-8	7.52287874528034	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	0	1	1	1
rs852069	3E-8	7.52287874528034	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs11871801	3E-8	7.52287874528034	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs356220	3E-8	7.52287874528034	21084426	Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.	Parkinson's disease	0	0	1	1
rs1733724	3E-8	7.52287874528034	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs10936599	3E-8	7.52287874528034	20972440	Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.	Colorectal cancer	0	1	1	1
rs206936	3E-8	7.52287874528034	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	1	1	1
rs12902421	3E-8	7.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs13177718	3E-8	7.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs822552	3E-8	7.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1046943	3E-8	7.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs7532866	3E-8	7.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs4605213	3E-8	7.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2279008	3E-8	7.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs5017948	3E-8	7.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	NA	NA	NA	NA
rs17780086	3E-8	7.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs8052560	3E-8	7.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs7567851	3E-8	7.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs4711336	3E-8	7.52287874528034	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs6569992	3E-8	7.52287874528034	20927387	A genome-wide association study of red blood cell traits using the electronic medical record.	Red blood cell traits	0	0	0	0
rs13048019	3E-8	7.52287874528034	20801718	Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.	Amyotrophic lateral sclerosis	1	1	1	1
rs17145713	3E-8	7.52287874528034	20802025	Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study.	Protein C levels	0	1	1	1
rs2858884	3E-8	7.52287874528034	20711174	Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy.	Narcolepsy	0	1	1	1
rs343064	3E-8	7.52287874528034	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs10128711	3E-8	7.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	1	1	1	1
rs7515577	3E-8	7.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Cholesterol, total	0	1	1	1
rs605066	3E-8	7.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	1	1
rs7941030	3E-8	7.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	0	0
rs1084651	3E-8	7.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	NA	NA	NA	NA
rs7255436	3E-8	7.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	0	1	1
rs645040	3E-8	7.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	1	1
rs11649653	3E-8	7.52287874528034	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	1	1
rs223116	3E-8	7.52287874528034	20639392	Genome-wide association analysis identifies multiple loci related to resting heart rate.	Resting heart rate	1	1	1	1
rs1701704	3E-8	7.52287874528034	20596022	Genome-wide association study in alopecia areata implicates both innate and adaptive immunity.	Alopecia areata	0	1	1	1
rs13292136	3E-8	7.52287874528034	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	1	1	1	1
rs1801214	3E-8	7.52287874528034	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	0	1	1	1
rs11642841	3E-8	7.52287874528034	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	0	0	1	1
rs8068952	3E-8	7.52287874528034	20548946	A genome-wide association study of optic disc parameters.	Vertical cup-disc ratio	1	1	1	1
rs1011970	3E-8	7.52287874528034	20453838	Genome-wide association study identifies five new breast cancer susceptibility loci.	Breast cancer	0	1	1	1
rs8192917	3E-8	7.52287874528034	20410501	Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.	Vitiligo	1	1	1	1
rs1006737	3E-8	7.52287874528034	20351715	Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.	Bipolar disorder and major depressive disorder (combined)	0	1	1	1
rs10091038	3E-8	7.52287874528034	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs2305480	3E-8	7.52287874528034	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	0	0	1	1
rs12928822	3E-8	7.52287874528034	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs1956529	3E-8	7.52287874528034	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (number of teeth)	0	1	1	1
rs35767	3E-8	7.52287874528034	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	0	0	0
rs35767	3E-8	7.52287874528034	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting insulin-related traits	0	0	0	0
rs4944092	3E-8	7.52287874528034	20062060	Genome-wide association study of PR interval.	PR interval	1	1	1	1
rs2229116	3E-8	7.52287874528034	20009918	A genome-wide association study of carotid atherosclerosis in HIV-infected men.	Carotid atherosclerosis in HIV infection	1	1	1	1
rs4311394	3E-8	7.52287874528034	20011104	A genome-wide association study reveals variants in ARL15 that influence adiponectin levels.	Adiponectin levels	1	1	1	1
rs886774	3E-8	7.52287874528034	19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Ulcerative colitis	0	0	1	1
rs1728785	3E-8	7.52287874528034	19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Ulcerative colitis	0	1	1	1
rs17181170	3E-8	7.52287874528034	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	1	1	1	1
rs2284063	3E-8	7.52287874528034	19578365	Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.	Cutaneous nevi	0	1	1	1
rs2605100	3E-8	7.52287874528034	19557161	Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.	Adiposity	0	1	1	1
rs7333181	3E-8	7.52287874528034	19448619	Loci at chromosomes 13, 19 and 20 influence age at natural menopause.	Menopause (age at onset)	1	1	1	1
rs4842838	3E-8	7.52287874528034	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs2201841	3E-8	7.52287874528034	19169254	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.	Psoriasis	0	1	1	1
rs6754295	3E-8	7.52287874528034	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Triglycerides	0	0	0	0
rs7819412	3E-8	7.52287874528034	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	Triglycerides	0	1	1	1
rs255049	3E-8	7.52287874528034	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	HDL cholesterol	0	0	1	1
rs2812378	3E-8	7.52287874528034	18794853	Common variants at CD40 and other loci confer risk of rheumatoid arthritis.	Rheumatoid arthritis	0	0	1	1
rs6478109	3E-8	7.52287874528034	18758464	Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.	Inflammatory bowel disease	0	0	1	1
rs678962	3E-8	7.52287874528034	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs185819	3E-8	7.52287874528034	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	1	1	1
rs4533267	3E-8	7.52287874528034	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs12986413	3E-8	7.52287874528034	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	0	0	1	1
rs2180341	3E-8	7.52287874528034	18326623	Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33.	Breast cancer	1	1	1	1
rs2660753	3E-8	7.52287874528034	18264097	Multiple newly identified loci associated with prostate cancer susceptibility.	Prostate cancer	1	1	1	1
rs16996148	3E-8	7.52287874528034	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	LDL cholesterol	0	0	0	0
rs2338104	3E-8	7.52287874528034	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs2794520	3E-8	7.52287874528034	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	0	1	1	1
rs1823068	3E-8	7.52287874528034	17903308	Genome-wide association of sleep and circadian phenotypes.	Sleepiness	1	1	1	1
rs12722489	3E-8	7.52287874528034	17660530	Risk alleles for multiple sclerosis identified by a genomewide study.	Multiple sclerosis	0	1	1	1
rs9930506	3E-8	7.52287874528034	17658951	Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits.	Obesity-related traits	0	1	1	1
rs6922269	3E-8	7.52287874528034	17634449	Genomewide association analysis of coronary artery disease.	Coronary heart disease	1	1	1	1
rs10801047	3E-8	7.52287874528034	17554261	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.	Crohn's disease	1	1	1	1
rs2542151	3E-8	7.52287874528034	17554261	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.	Crohn's disease	0	0	1	1
rs7309	4E-8	7.39794000867204	23722424	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.	Educational attainment	1	1	1	1
rs4937076	4E-8	7.39794000867204	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (time to first tooth eruption)	1	1	1	1
rs6042507	4E-8	7.39794000867204	23620142	Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.	Circulating myeloperoxidase levels (serum) 	1	1	1	1
rs1516725	4E-8	7.39794000867204	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Body mass index	0	0	0	0
rs1594829	4E-8	7.39794000867204	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Height	1	1	1	1
rs2531995	4E-8	7.39794000867204	23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Obesity	1	1	1	1
rs6922617	4E-8	7.39794000867204	23562540	GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.	Alzheimer's disease biomarkers	1	1	1	1
rs2427345	4E-8	7.39794000867204	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	1	1	1	1
rs11075995	4E-8	7.39794000867204	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	1	1	1	1
rs9790517	4E-8	7.39794000867204	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	0	1	1	1
rs12422552	4E-8	7.39794000867204	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs10206899	4E-8	7.39794000867204	23535967	Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate.	Glomerular filtration rate	0	0	0	0
rs8045064	4E-8	7.39794000867204	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs2799573	4E-8	7.39794000867204	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs12576775	4E-8	7.39794000867204	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs10503253	4E-8	7.39794000867204	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs6565887	4E-8	7.39794000867204	23432519	A genome-wide association study of recipient genotype and medium-term kidney allograft function.	Renal transplant outcome	1	1	1	1
rs7042950	4E-8	7.39794000867204	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs278541	4E-8	7.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4878639	4E-8	7.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1049110	4E-8	7.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs9296009	4E-8	7.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs7973719	4E-8	7.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6583437	4E-8	7.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6722456 	4E-8	7.39794000867204	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	NA	NA	NA	NA
rs12289961	4E-8	7.39794000867204	23349640	Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.	Lymphoma	0	1	1	1
rs17482078	4E-8	7.39794000867204	23291587	Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.	Behcet's disease	0	0	0	0
rs3931397	4E-8	7.39794000867204	23291589	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.	Corneal structure	1	1	1	1
rs2022309	4E-8	7.39794000867204	23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	End-stage coagulation	0	1	1	1
rs367615	4E-8	7.39794000867204	23300701	Genome-wide search for gene-gene interactions in colorectal cancer.	Colorectal cancer	1	1	1	1
rs11903757	4E-8	7.39794000867204	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	1	1	1	1
rs12447804	4E-8	7.39794000867204	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	1	1	1	1
rs1728785	4E-8	7.39794000867204	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Ulcerative colitis	0	0	1	1
rs1668357	4E-8	7.39794000867204	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	0	1	1	1
rs729302	4E-8	7.39794000867204	23053960	Genome-wide pathway analysis of genome-wide association studies on systemic lupus erythematosus and rheumatoid arthritis.	Systemic lupus erythematosus	0	1	1	1
rs9733352	4E-8	7.39794000867204	23031429	A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol.	Apolipoprotein Levels	1	1	1	1
rs8100241	4E-8	7.39794000867204	22976474	A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.	Breast cancer	0	0	1	1
rs6475606	4E-8	7.39794000867204	22961961	Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk.	Intracranial aneurysm	0	0	1	1
rs12059546	4E-8	7.39794000867204	22949513	Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32	Epilepsy (generalized)	1	1	1	1
rs7632427	4E-8	7.39794000867204	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs6618677	4E-8	7.39794000867204	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	NA	NA	NA	NA
rs2469184	4E-8	7.39794000867204	22703881	Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.	Activated partial thromboplastin time	1	1	1	1
rs7709645	4E-8	7.39794000867204	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	1	1	1	1
rs6478241	4E-8	7.39794000867204	22683712	Genome-wide association analysis identifies susceptibility loci for migraine without aura.	Migraine	1	1	1	1
rs3802177	4E-8	7.39794000867204	22693455	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.	Type 2 diabetes	0	0	1	1
rs9408926	4E-8	7.39794000867204	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	0	0	0	0
rs6728021	4E-8	7.39794000867204	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune response to smallpox vaccine (IL-6)	1	1	1	1
rs4646949	4E-8	7.39794000867204	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	0	1	1	1
rs3814231	4E-8	7.39794000867204	22561518	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.	Vitiligo	1	1	1	1
rs1129038	4E-8	7.39794000867204	22561518	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.	Vitiligo	0	1	1	1
rs12901682	4E-8	7.39794000867204	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs3001032	4E-8	7.39794000867204	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	1	1	1
rs7955516	4E-8	7.39794000867204	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	1	1	1	1
rs6431731	4E-8	7.39794000867204	22479191	Genome-wide association and functional follow-up reveals new loci for kidney function.	Chronic kidney disease	1	1	1	1
rs3091316	4E-8	7.39794000867204	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	0	0	1	1
rs3091338	4E-8	7.39794000867204	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	0	0	1	1
rs4846922	4E-8	7.39794000867204	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	1	1	1
rs782590	4E-8	7.39794000867204	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	1	1	1	1
rs6711016	4E-8	7.39794000867204	22399527	Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.	Metabolic syndrome	0	0	0	0
rs416350	4E-8	7.39794000867204	22365631	Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.	Temperament (bipolar disorder)	1	1	1	1
rs1424760	4E-8	7.39794000867204	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs17148090	4E-8	7.39794000867204	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	1	1	1	1
rs2897442	4E-8	7.39794000867204	22197932	Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis.	Atopic dermatitis	0	1	1	1
rs4775302	4E-8	7.39794000867204	22130093	New variants at 10q26 and 15q21 are associated with aggressive prostate cancer in a genome-wide association study from a prostate biopsy screening cohort.	Prostate cancer	1	1	1	1
rs12722489	4E-8	7.39794000867204	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs2293152	4E-8	7.39794000867204	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	NA	NA	NA	NA
rs10076782	4E-8	7.39794000867204	22139419	New gene functions in megakaryopoiesis and platelet formation.	Mean platelet volume	0	1	1	1
rs7565981	4E-8	7.39794000867204	22137330	Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.	Creutzfeldt-Jakob disease (variant)	1	1	1	1
rs719714	4E-8	7.39794000867204	22126837	Genome-wide study identifies PTPRO and WDR72 and FOXQ1-SUMO1P1 interaction associated with neurocognitive function.	Cognitive function	1	1	1	1
rs1945213	4E-8	7.39794000867204	22076464	Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	0	0	0	0
rs2523809	4E-8	7.39794000867204	22075330	A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study.	IgE levels 	0	1	1	1
rs1497406	4E-8	7.39794000867204	22010049	Loci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations.	Gamma gluatamyl transferase levels	0	1	1	1
rs2155219	4E-8	7.39794000867204	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	Allergic rhinitis	0	1	0	0
rs12447804	4E-8	7.39794000867204	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	1	1	1
rs2075650	4E-8	7.39794000867204	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	0	0	0	0
rs12576775	4E-8	7.39794000867204	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	0	1	1	1
rs1327235	4E-8	7.39794000867204	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs12212193	4E-8	7.39794000867204	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs12048904	4E-8	7.39794000867204	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	0	0	0
rs2121875	4E-8	7.39794000867204	21743467	Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.	Prostate cancer	1	1	1	1
rs2292884	4E-8	7.39794000867204	21743057	Genome-wide association study identifies new prostate cancer susceptibility loci.	Prostate cancer	0	0	1	1
rs6599389	4E-8	7.39794000867204	21738487	Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.	Parkinson's disease	0	0	1	1
rs822354	4E-8	7.39794000867204	21700879	Novel locus FER is associated with serum HMW adiponectin levels.	Adiponectin levels	1	1	1	1
rs1559040	4E-8	7.39794000867204	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs4621553	4E-8	7.39794000867204	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs569214	4E-8	7.39794000867204	21627779	The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease.	Alzheimer's disease	0	0	1	1
rs1412444	4E-8	7.39794000867204	21606135	A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.	Coronary heart disease	1	1	1	1
rs11088859	4E-8	7.39794000867204	21552555	A genome-wide association study on obesity and obesity-related traits.	Obesity	1	1	1	1
rs6943555	4E-8	7.39794000867204	21471458	Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption.	Alcohol consumption	1	1	1	1
rs6974491	4E-8	7.39794000867204	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	1	1	1	1
rs9987289	4E-8	7.39794000867204	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	1	0	0
rs2266788	4E-8	7.39794000867204	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Triglycerides-Blood Pressure (TG-BP)	0	0	0	0
rs9419788	4E-8	7.39794000867204	21368711	Genome-wide association study of personality traits in bipolar patients.	Personality dimensions	1	1	1	1
rs6499188	4E-8	7.39794000867204	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	0	1	1
rs3194051	4E-8	7.39794000867204	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs735396	4E-8	7.39794000867204	21203500	Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation.	N-glycan levels	0	0	0	0
rs6720394	4E-8	7.39794000867204	21151127	Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci.	Primary sclerosing cholangitis	0	1	1	1
rs6568421	4E-8	7.39794000867204	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs8050136	4E-8	7.39794000867204	21037115	Genome-wide association analysis of body mass in chronic obstructive pulmonary disease.	Body mass in chronic obstructive pulmonary disease	0	1	1	1
rs12201676	4E-8	7.39794000867204	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1967017	4E-8	7.39794000867204	20884846	Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.	Urate levels	0	0	1	1
rs955748	4E-8	7.39794000867204	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2072153	4E-8	7.39794000867204	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs6892884	4E-8	7.39794000867204	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs1367226	4E-8	7.39794000867204	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	0	0	0
rs4676049	4E-8	7.39794000867204	20885792	Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.	Alzheimer's disease (late onset)	1	1	1	1
rs2304130	4E-8	7.39794000867204	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	Triglycerides	0	0	0	0
rs6484218	4E-8	7.39794000867204	20713499	Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression.	Schizophrenia, bipolar disorder and depression (combined)	1	1	1	1
rs7134375	4E-8	7.39794000867204	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	1	1
rs5756931	4E-8	7.39794000867204	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	Triglycerides	0	1	1	1
rs4141463	4E-8	7.39794000867204	20663923	A genome-wide scan for common alleles affecting risk for autism.	Autism	1	1	1	1
rs7682241	4E-8	7.39794000867204	20596022	Genome-wide association study in alopecia areata implicates both innate and adaptive immunity.	Alopecia areata	0	1	1	1
rs494453	4E-8	7.39794000867204	20548944	An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.	Osteoporosis	1	1	1	1
rs26232	4E-8	7.39794000867204	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	1	1	1	1
rs12286037	4E-8	7.39794000867204	20442857	Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study.	Lipoprotein-associated phospholipase A2 activity and mass	0	0	1	1
rs3025343	4E-8	7.39794000867204	20418890	Genome-wide meta-analyses identify multiple loci associated with smoking behavior.	Smoking behavior	1	1	1	1
rs7593730	4E-8	7.39794000867204	20418489	Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes.	Type 2 diabetes	1	1	1	1
rs2500535	4E-8	7.39794000867204	20360315	Genome-wide pharmacogenetics of antidepressant response in the GENDEP project.	Response to antidepressants	1	1	1	1
rs5771069	4E-8	7.39794000867204	20228798	Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL).	Ulcerative colitis	1	1	1	1
rs11071657	4E-8	7.39794000867204	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	1	1	1
rs17085106	4E-8	7.39794000867204	19656524	A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.	Orofacial clefts	1	1	1	1
rs2478333	4E-8	7.39794000867204	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	QT interval	1	1	1	1
rs885389	4E-8	7.39794000867204	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs881375	4E-8	7.39794000867204	19503088	REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.	Rheumatoid arthritis	0	0	1	1
rs855913	4E-8	7.39794000867204	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs4948088	4E-8	7.39794000867204	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs2384550	4E-8	7.39794000867204	19430479	Genome-wide association study of blood pressure and hypertension.	Diastolic blood pressure	0	1	1	1
rs6754295	4E-8	7.39794000867204	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	HDL cholesterol	0	0	0	0
rs4846914	4E-8	7.39794000867204	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	HDL cholesterol	0	0	1	1
rs11206510	4E-8	7.39794000867204	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	LDL cholesterol	0	0	1	1
rs7120118	4E-8	7.39794000867204	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	HDL cholesterol	0	1	1	1
rs700651	4E-8	7.39794000867204	18997786	Susceptibility loci for intracranial aneurysm in European and Japanese populations.	Intracranial aneurysm	0	1	1	1
rs2040704	4E-8	7.39794000867204	18846228	Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus.	IgE levels 	0	0	1	1
rs1121980	4E-8	7.39794000867204	18454148	Common variants near MC4R are associated with fat mass, weight and risk of obesity.	Body mass index	0	0	1	1
rs4713858	4E-8	7.39794000867204	18391951	Many sequence variants affecting diversity of adult human height.	Height	1	1	1	1
rs10923931	4E-8	7.39794000867204	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	0	1	1	1
rs1970546	4E-8	7.39794000867204	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Volumetric brain MRI	1	1	1	1
rs9858542	4E-8	7.39794000867204	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Crohn's disease	0	0	1	1
rs380390	4E-8	7.39794000867204	15761122	Complement factor H polymorphism in age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs13135284	5E-8	7.30102999566398	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (parent-of-origin)	1	1	1	1
rs1561288	5E-8	7.30102999566398	23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Body mass index	0	0	1	1
rs7010162	5E-8	7.30102999566398	23666240	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.	Testicular germ cell tumor	1	1	1	1
rs4140885	5E-8	7.30102999566398	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs6975557	5E-8	7.30102999566398	23593202	Bivariate genome-wide association analyses identified genes with pleiotropic effects for femoral neck bone geometry and age at menarche.	Femoral neck bone geometry and menarche (age at onset)	1	1	1	1
rs6869841	5E-8	7.30102999566398	23535732	Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.	Prostate cancer	0	1	1	1
rs12710696	5E-8	7.30102999566398	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	1	1	1	1
rs11571833	5E-8	7.30102999566398	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	1	1	1	1
rs12202284	5E-8	7.30102999566398	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Non-melanoma skin cancer	0	1	1	1
rs61144803	5E-8	7.30102999566398	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs281379	5E-8	7.30102999566398	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs17662626	5E-8	7.30102999566398	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs7860634	5E-8	7.30102999566398	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs6499766	5E-8	7.30102999566398	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	1	1	1	1
rs10065906	5E-8	7.30102999566398	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs12342831	5E-8	7.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10813957	5E-8	7.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7652995	5E-8	7.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs3788556	5E-8	7.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11622412	5E-8	7.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA/ MHPG Ratio)	1	1	1	1
rs10852344	5E-8	7.30102999566398	23307926	A genome-wide association study of early menopause and the combined impact of identified variants.	Menopause (age at onset)	0	0	1	1
rs836132	5E-8	7.30102999566398	23279374	Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain.	β2-Glycoprotein I (β2-GPI) plasma levels	1	1	1	1
rs877282	5E-8	7.30102999566398	23703922	A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls.	Uric acid levels	1	1	1	1
rs11001819	5E-8	7.30102999566398	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs12564445	5E-8	7.30102999566398	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	1	1	1	1
rs4432842	5E-8	7.30102999566398	23202124	New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.	Birth weight	1	1	1	1
rs913678	5E-8	7.30102999566398	23128233	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Inflammatory bowel disease	1	1	1	1
rs8039584	5E-8	7.30102999566398	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs13407662	5E-8	7.30102999566398	23041239	Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.	Stroke (ischemic)	1	1	1	1
rs12608932	5E-8	7.30102999566398	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	0	0	1	1
rs11037575	5E-8	7.30102999566398	22941191	Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.	Neuroblastoma	1	1	1	1
rs556621	5E-8	7.30102999566398	22941190	Common variants at 6p21.1 are associated with large artery atherosclerotic stroke.	Stroke (ischemic)	1	1	1	1
rs1795240	5E-8	7.30102999566398	22903471	Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.	Lentiform nucleus volume 	1	1	1	1
rs62314947	5E-8	7.30102999566398	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs9850225	5E-8	7.30102999566398	22704111	Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.	Erectile dysfunction	1	1	1	1
rs2298948	5E-8	7.30102999566398	22745009	Multiple loci influencing hippocampal degeneration identified by genome scan.	Hippocampal atrophy	1	1	1	1
rs11121380	5E-8	7.30102999566398	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs12565755	5E-8	7.30102999566398	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs4831760	5E-8	7.30102999566398	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs12726330	5E-8	7.30102999566398	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	1	1	1	1
rs9437689	5E-8	7.30102999566398	22359512	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Phospholipid levels (plasma)	0	1	1	1
rs7616006	5E-8	7.30102999566398	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs7638110	5E-8	7.30102999566398	22013104	Genome-wide scan for loci of adolescent obesity and their relationship with blood pressure.	Obesity and blood pressure	1	1	1	1
rs6703335	5E-8	7.30102999566398	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	1	1	1	1
rs17662626	5E-8	7.30102999566398	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	1	1	1
rs12214416	5E-8	7.30102999566398	21900290	Genetic variants, plasma lipoprotein(a) levels, and risk of cardiovascular morbidity and mortality among two prospective cohorts of type 2 diabetes.	Lp (a) levels	1	1	1	1
rs8070463	5E-8	7.30102999566398	21743469	Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.	Ankylosing spondylitis	0	1	1	1
rs10447248	5E-8	7.30102999566398	21700879	Novel locus FER is associated with serum HMW adiponectin levels.	Adiponectin levels	1	1	1	1
rs4363657	5E-8	7.30102999566398	21646302	Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels.	Bilirubin levels	0	0	1	1
rs300774	5E-8	7.30102999566398	21423239	A genome-wide association study of attempted suicide.	Suicide attempts in bipolar disorder	1	1	1	1
rs11984075	5E-8	7.30102999566398	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	0	1	1	1
rs6901250	5E-8	7.30102999566398	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	1	1	1	1
rs757647	5E-8	7.30102999566398	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs7853377	5E-8	7.30102999566398	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs2421992	5E-8	7.30102999566398	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	0	1	1
rs17342717	5E-8	7.30102999566398	20927387	A genome-wide association study of red blood cell traits using the electronic medical record.	Red blood cell traits	0	0	0	0
rs7044529	5E-8	7.30102999566398	20719862	New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.	Central corneal thickness	0	1	1	1
rs2923084	5E-8	7.30102999566398	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	1	1
rs6450176	5E-8	7.30102999566398	20686565	Biological, clinical and population relevance of 95 loci for blood lipids.	HDL cholesterol	0	1	1	1
rs2893923	5E-8	7.30102999566398	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	0	1	1	1
rs13315591	5E-8	7.30102999566398	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	1	1	1	1
rs4077515	5E-8	7.30102999566398	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	0	0	1	1
rs17291045	5E-8	7.30102999566398	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs9368699	5E-8	7.30102999566398	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	0	0	0	0
rs4466998	5E-8	7.30102999566398	19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Mean corpuscular volume	0	1	1	1
rs599083	5E-8	7.30102999566398	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	0	1	1	1
rs4234898	5E-8	7.30102999566398	19786962	First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children.	Speech perception in dyslexia	1	1	1	1
rs9473555	5E-8	7.30102999566398	19744961	Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.	Folate pathway vitamin levels	1	1	1	1
rs1569019	5E-8	7.30102999566398	19729412	Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs.	Height	1	1	1	1
rs505922	5E-8	7.30102999566398	19648918	Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer.	Pancreatic cancer	0	1	1	1
rs10146997	5E-8	7.30102999566398	19557197	NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium.	Waist circumference	0	1	1	1
rs2153157	5E-8	7.30102999566398	19448621	Genome-wide association studies identify loci associated with age at menarche and age at natural menopause.	Menarche and menopause (age at onset)	0	1	1	1
rs11755527	5E-8	7.30102999566398	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	0	1	1
rs13437082	5E-8	7.30102999566398	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs3742207	5E-8	7.30102999566398	20031579	COL4A1 is associated with arterial stiffness by genome-wide association scan.	Arterial stiffness	1	1	1	1
rs6773957	5E-8	7.30102999566398	19165155	Genome-wide linkage and association analyses to identify genes influencing adiponectin levels: the GEMS Study.	Adiponectin levels	1	1	1	1
rs13266634	5E-8	7.30102999566398	19096518	Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study.	Glycated hemoglobin levels	0	1	1	1
rs157580	5E-8	7.30102999566398	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	LDL cholesterol	0	0	1	1
rs10096633	5E-8	7.30102999566398	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	Metabolic traits	0	1	1	1
rs174548	5E-8	7.30102999566398	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	0	0	1	1
rs7846385	5E-8	7.30102999566398	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs2254287	5E-8	7.30102999566398	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	LDL cholesterol	0	1	1	1
rs10260404	5E-8	7.30102999566398	18084291	Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs7903146	5E-8	7.30102999566398	17668382	Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium.	Type 2 diabetes	0	0	1	1
rs3764021	5E-8	7.30102999566398	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 1 diabetes	0	0	1	1
rs9858542	5E-8	7.30102999566398	17554261	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.	Crohn's disease	0	0	1	1
rs13266634	5E-8	7.30102999566398	17463246	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	Type 2 diabetes	0	0	1	1
rs10811661	5E-8	7.30102999566398	17463246	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	Type 2 diabetes	0	0	1	1
rs13266634	5E-8	7.30102999566398	17463248	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.	Type 2 diabetes	0	0	1	1
rs13266634	5E-8	7.30102999566398	17463249	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs2273359	6E-8	7.22184874961636	23753411	Genomic association analysis of common variants influencing antihypertensive response to hydrochlorothiazide.	Response to diuretic therapy in hypertension	1	1	1	1
rs4819833	6E-8	7.22184874961636	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (parent-of-origin)	1	1	1	1
rs1011970	6E-8	7.22184874961636	23535729	Large-scale genotyping identifies 41 new loci associated with breast cancer risk.	Breast cancer	0	0	1	1
rs6757804	6E-8	7.22184874961636	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	1	1	1	1
rs2859113	6E-8	7.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs3217810	6E-8	7.22184874961636	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	NA	NA	NA	NA
rs1260326	6E-8	7.22184874961636	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum total protein level	0	1	0	0
rs10097731	6E-8	7.22184874961636	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum total protein level	1	1	1	1
rs7744666	6E-8	7.22184874961636	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs11969002	6E-8	7.22184874961636	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs72829446	6E-8	7.22184874961636	22936694	Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men.	Androgen levels	0	0	0	0
rs7004633	6E-8	7.22184874961636	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	0	1	1	1
rs11757063	6E-8	7.22184874961636	22683712	Genome-wide association analysis identifies susceptibility loci for migraine without aura.	Migraine	1	1	1	1
rs6016142	6E-8	7.22184874961636	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Estradiol levels	1	1	1	1
rs11708067	6E-8	7.22184874961636	22693455	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.	Type 2 diabetes	0	1	1	1
rs11242417	6E-8	7.22184874961636	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-12p40)	0	1	1	1
rs17168526	6E-8	7.22184874961636	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-1beta)	NA	NA	NA	NA
rs10432496	6E-8	7.22184874961636	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	1	1	1	1
rs9922619	6E-8	7.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	0	1	1	1
rs9807989	6E-8	7.22184874961636	22561531	Genome-wide association study to identify genetic determinants of severe asthma.	Asthma	0	0	1	1
rs6450176	6E-8	7.22184874961636	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	0	1	1
rs7838490	6E-8	7.22184874961636	22417934	Genome-wide association study identifies genetic loci associated with body mass index and high density lipoprotein-cholesterol levels during psychopharmacological treatment - a cross-sectional naturalistic study.	Body mass index and cholesterol (psychopharmacological treatment)	0	1	1	1
rs12563333	6E-8	7.22184874961636	22205951	Genome-wide association study in bipolar patients stratified by co-morbidity.	Bipolar disorder	1	1	1	1
rs6141	6E-8	7.22184874961636	22139419	New gene functions in megakaryopoiesis and platelet formation.	Platelet counts	1	1	1	1
rs2239547	6E-8	7.22184874961636	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	1	1	1
rs7129220	6E-8	7.22184874961636	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	0	1	0	0
rs4308217	6E-8	7.22184874961636	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs11171747	6E-8	7.22184874961636	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	1	1	1
rs11868035	6E-8	7.22184874961636	21738487	Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.	Parkinson's disease	0	1	1	1
rs6687758	6E-8	7.22184874961636	21685912	Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.	Progressive supranuclear palsy	0	1	1	1
rs2281680	6E-8	7.22184874961636	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs10468017	6E-8	7.22184874961636	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	0	0	0
rs11129640	6E-8	7.22184874961636	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Entorhinal cortical thickness	1	1	1	1
rs9555810	6E-8	7.22184874961636	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs16938437	6E-8	7.22184874961636	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs4730250	6E-8	7.22184874961636	21068099	Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22.	Osteoarthritis	1	1	1	1
rs2922763	6E-8	7.22184874961636	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	1	1	1
rs11206801	6E-8	7.22184874961636	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	AB1-42	1	1	1	1
rs1168013	6E-8	7.22184874961636	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs2301436	6E-8	7.22184874961636	20570966	Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.	Crohn's disease	0	0	1	1
rs12025126	6E-8	7.22184874961636	20548946	A genome-wide association study of optic disc parameters.	Vertical cup-disc ratio	0	1	1	1
rs710521	6E-8	7.22184874961636	20348956	A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.	Urinary bladder cancer	0	1	1	1
rs1033180	6E-8	7.22184874961636	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	1	1	1	1
rs5979785	6E-8	7.22184874961636	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	NA	NA	NA	NA
rs1876040	6E-8	7.22184874961636	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs11012	6E-8	7.22184874961636	20070850	Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.	Parkinson's disease	0	0	1	1
rs11014166	6E-8	7.22184874961636	19430479	Genome-wide association study of blood pressure and hypertension.	Hypertension	0	1	0	0
rs11809207	6E-8	7.22184874961636	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	1	1	1	1
rs10484554	6E-8	7.22184874961636	19115949	Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02).	AIDS progression	0	1	1	1
rs13194984	6E-8	7.22184874961636	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	1	1	1	1
rs10913469	6E-8	7.22184874961636	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Body mass index	0	0	0	0
rs2815752	6E-8	7.22184874961636	19079261	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.	Body mass index	0	0	1	1
rs1460163	6E-8	7.22184874961636	19081515	Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.	Creutzfeldt-Jakob disease	1	1	1	1
rs1447352	6E-8	7.22184874961636	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	Metabolic traits	0	1	1	1
rs11243897	6E-8	7.22184874961636	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs6918152	6E-8	7.22184874961636	18483556	A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.	Black vs. blond hair color	1	1	1	1
rs757608	6E-8	7.22184874961636	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs2562784	6E-8	7.22184874961636	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	1	1	1	1
rs420259	6E-8	7.22184874961636	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Bipolar disorder	0	0	1	1
rs10883365	6E-8	7.22184874961636	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Crohn's disease	0	0	1	1
rs9300039	6E-8	7.22184874961636	17463248	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.	Type 2 diabetes	1	1	1	1
rs13266634	6E-8	7.22184874961636	17293876	A genome-wide association study identifies novel risk loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs17702901	7E-8	7.15490195998574	23643386	Weight loss after gastric bypass is associated with a variant at 15q26.1.	Weight loss (gastric bypass surgery)	1	1	1	1
rs3002288	7E-8	7.15490195998574	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Eye color	1	1	1	1
rs8015138	7E-8	7.15490195998574	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Non-melanoma skin cancer	1	1	1	1
rs12091371	7E-8	7.15490195998574	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs143258881	7E-8	7.15490195998574	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs10813951	7E-8	7.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11654749	7E-8	7.15490195998574	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	0	0	0
rs6723108	7E-8	7.15490195998574	23209189	Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21.	Type 2 diabetes	0	1	1	1
rs3114018	7E-8	7.15490195998574	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs2280401	7E-8	7.15490195998574	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum total protein level	0	1	0	0
rs3011225	7E-8	7.15490195998574	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis (age of onset)	1	1	1	1
rs780093	7E-8	7.15490195998574	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	0	0	0
rs440837	7E-8	7.15490195998574	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	0	0	0
rs9835973	7E-8	7.15490195998574	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-1beta)	1	1	1	1
rs13414205	7E-8	7.15490195998574	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted TNF-alpha)	NA	NA	NA	NA
rs6905288	7E-8	7.15490195998574	22319020	A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.	Coronary heart disease	0	1	1	1
rs200113	7E-8	7.15490195998574	22229870	Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia.	Uric acid levels	1	1	1	1
rs3769124	7E-8	7.15490195998574	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	NA	NA	NA	NA
rs534870	7E-8	7.15490195998574	21706003	Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.	Adiposity	1	1	1	1
rs11568563	7E-8	7.15490195998574	21685912	Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.	Progressive supranuclear palsy	1	1	1	1
rs9394152	7E-8	7.15490195998574	21685187	Genome-wide association study of smoking behaviours in patients with COPD.	Chronic obstructive pulmonary disease	0	1	1	1
rs114216682	7E-8	7.15490195998574	21685187	Genome-wide association study of smoking behaviours in patients with COPD.	Chronic obstructive pulmonary disease	1	1	1	1
rs11979158	7E-8	7.15490195998574	21531791	Chromosome 7p11.2 (EGFR) variation influences glioma risk.	Glioma	1	1	1	1
rs3768080	7E-8	7.15490195998574	21478494	Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk.	Cutaneous nevi	1	1	1	1
rs7385804	7E-8	7.15490195998574	21208937	Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.	Iron levels	0	1	1	1
rs286913	7E-8	7.15490195998574	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Response to antipsychotic treatment	1	1	1	1
rs501764	7E-8	7.15490195998574	21037568	A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).	Hodgkin's lymphoma	1	1	1	1
rs4649203	7E-8	7.15490195998574	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	1	1	1	1
rs2745967	7E-8	7.15490195998574	20639392	Genome-wide association analysis identifies multiple loci related to resting heart rate.	Resting heart rate	0	1	1	1
rs11154022	7E-8	7.15490195998574	20639392	Genome-wide association analysis identifies multiple loci related to resting heart rate.	Resting heart rate	0	1	1	1
rs10045431	7E-8	7.15490195998574	20570966	Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.	Crohn's disease	0	0	1	1
rs11172782	7E-8	7.15490195998574	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	1	1	1	1
rs2736990	7E-8	7.15490195998574	20070850	Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.	Parkinson's disease	0	0	1	1
rs1733724	7E-8	7.15490195998574	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	1	1	1
rs9497975	7E-8	7.15490195998574	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	NA	NA	NA	NA
rs38152	7E-8	7.15490195998574	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs8013190	7E-8	7.15490195998574	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	NA	NA	NA	NA
rs823128	7E-8	7.15490195998574	19915575	Genome-wide association study reveals genetic risk underlying Parkinson's disease.	Parkinson's disease	1	1	1	1
rs17115100	7E-8	7.15490195998574	19915575	Genome-wide association study reveals genetic risk underlying Parkinson's disease.	Parkinson's disease	0	1	1	1
rs1268789	7E-8	7.15490195998574	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	1	1	1	1
rs12517906	7E-8	7.15490195998574	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Weight	1	1	1	1
rs154659	7E-8	7.15490195998574	19340012	Genome-wide association study of tanning phenotype in a population of European ancestry.	Tanning	0	1	1	1
rs1006737	7E-8	7.15490195998574	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	0	0	1	1
rs10958476	7E-8	7.15490195998574	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs10935120	7E-8	7.15490195998574	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	1	1	1	1
rs5015480	7E-8	7.15490195998574	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs1738074	7E-8	7.15490195998574	18311140	Newly identified genetic risk variants for celiac disease related to the immune response.	Celiac disease	0	0	1	1
rs1463605	7E-8	7.15490195998574	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Aging traits	1	1	1	1
rs1397048	7E-8	7.15490195998574	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	0	1	1	1
rs3783006	8E-8	7.09691001300806	23722424	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.	Educational attainment	1	1	1	1
rs1048466	8E-8	7.09691001300806	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	1	1	1	1
rs4794202	8E-8	7.09691001300806	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs2046315	8E-8	7.09691001300806	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Smooth-surface caries 	1	1	1	1
rs7762544	8E-8	7.09691001300806	23459936	Exploring the genetic basis of chronic periodontitis: a genome-wide association study.	Periodontitis	1	1	1	1
rs3811321	8E-8	7.09691001300806	23432519	A genome-wide association study of recipient genotype and medium-term kidney allograft function.	Renal transplant outcome	1	1	1	1
rs161645	8E-8	7.09691001300806	23290196	A genome-wide association study of depressive symptoms.	Depression (quantitative trait)	1	1	1	1
rs2244608	8E-8	7.09691001300806	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs2857595	8E-8	7.09691001300806	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs8056446   	8E-8	7.09691001300806	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs2293579	8E-8	7.09691001300806	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	0	1	1	1
rs11574703	8E-8	7.09691001300806	22890011	Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate.	Response to fenofibrate	1	1	1	1
rs8023580	8E-8	7.09691001300806	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	0	0	0
rs2075650	8E-8	7.09691001300806	22694956	Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.	Age-related macular degeneration	0	0	1	1
rs13025591	8E-8	7.09691001300806	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	1	1	1	1
rs210359	8E-8	7.09691001300806	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs13067593	8E-8	7.09691001300806	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs738968	8E-8	7.09691001300806	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted TNF-alpha)	1	1	1	1
rs1516489	8E-8	7.09691001300806	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune response to smallpox vaccine (IL-6)	1	1	1	1
rs10248619	8E-8	7.09691001300806	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	1	1	1	1
rs2546890	8E-8	7.09691001300806	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs4712972	8E-8	7.09691001300806	21909108	Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.	Carotid intima media thickness	0	1	1	1
rs2744148	8E-8	7.09691001300806	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs1145652	8E-8	7.09691001300806	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs10792320	8E-8	7.09691001300806	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs6704644	8E-8	7.09691001300806	21646302	Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels.	Bilirubin levels	1	1	1	1
rs2252586	8E-8	7.09691001300806	21531791	Chromosome 7p11.2 (EGFR) variation influences glioma risk.	Glioma	1	1	1	1
rs17126232	8E-8	7.09691001300806	21552555	A genome-wide association study on obesity and obesity-related traits.	Obesity	1	1	1	1
rs1532278	8E-8	7.09691001300806	21460841	Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.	Alzheimer's disease (late onset)	0	1	1	1
rs6943029	8E-8	7.09691001300806	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	1	1	1	1
rs4598195	8E-8	7.09691001300806	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	0	0	1	1
rs3815148	8E-8	7.09691001300806	20112360	A genome-wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22.	Osteoarthritis	0	0	1	1
rs3815087	8E-8	7.09691001300806	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	0	1	1	1
rs2395730	8E-8	7.09691001300806	20010834	Genome-wide association study identifies five loci associated with lung function.	Pulmonary function	1	1	1	1
rs3024493	8E-8	7.09691001300806	19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Ulcerative colitis	0	0	1	1
rs982393	8E-8	7.09691001300806	19744961	Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.	Folate pathway vitamin levels	1	1	1	1
rs13266634	8E-8	7.09691001300806	19734900	Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia.	Type 2 diabetes and other traits	0	1	1	1
rs2089222	8E-8	7.09691001300806	19684603	Germline genomic variants associated with childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs3825932	8E-8	7.09691001300806	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	0	1	1
rs1918974	8E-8	7.09691001300806	19430483	Genome-wide association study identifies eight loci associated with blood pressure.	Diastolic blood pressure	0	0	1	1
rs8041863	8E-8	7.09691001300806	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	1	1	1	1
rs4402960	8E-8	7.09691001300806	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs653178	8E-8	7.09691001300806	18311140	Newly identified genetic risk variants for celiac disease related to the immune response.	Celiac disease	0	0	1	1
rs1528753	8E-8	7.09691001300806	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Aging traits	1	1	1	1
rs10484246	8E-8	7.09691001300806	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Morbidity-free survival	1	1	1	1
rs2075555	8E-8	7.09691001300806	17903305	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	Breast cancer	1	1	1	1
rs7775861	9E-8	7.04575749056067	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (non-asthmatics)	0	1	1	1
rs9469890	9E-8	7.04575749056067	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs300032	9E-8	7.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs12461110	9E-8	7.04575749056067	23307926	A genome-wide association study of early menopause and the combined impact of identified variants.	Menopause (age at onset)	0	0	1	1
rs2388896	9E-8	7.04575749056067	23297363	Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.	Tetralogy of Fallot	1	1	1	1
rs10911251	9E-8	7.04575749056067	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	1	1	1	1
rs8040868   	9E-8	7.04575749056067	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs4141819	9E-8	7.04575749056067	23104006	Genome-wide association meta-analysis identifies new endometriosis risk loci.	Endometriosis	1	1	1	1
rs6457690	9E-8	7.04575749056067	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs1029296	9E-8	7.04575749056067	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs11128603	9E-8	7.04575749056067	22990020	Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation.	Plasminogen activator inhibitor type 1 levels (PAI-1)	1	1	1	1
rs305061	9E-8	7.04575749056067	22700719	Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.	Chronic lymphocytic leukemia	1	1	1	1
rs1584468	9E-8	7.04575749056067	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-12p40)	1	1	1	1
rs10885122	9E-8	7.04575749056067	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs8182584	9E-8	7.04575749056067	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	0	1	1	1
rs6510827	9E-8	7.04575749056067	22561518	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.	Vitiligo	1	1	1	1
rs11615274	9E-8	7.04575749056067	22417934	Genome-wide association study identifies genetic loci associated with body mass index and high density lipoprotein-cholesterol levels during psychopharmacological treatment - a cross-sectional naturalistic study.	Body mass index and cholesterol (psychopharmacological treatment)	1	1	1	1
rs3736830	9E-8	7.04575749056067	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs13432159	9E-8	7.04575749056067	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	1	1	1	1
rs3219090	9E-8	7.04575749056067	21983785	Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3.	Melanoma	1	1	1	1
rs4373814	9E-8	7.04575749056067	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Hypertension	0	1	0	0
rs180515	9E-8	7.04575749056067	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs3821236	9E-8	7.04575749056067	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	0	1	1
rs4389526	9E-8	7.04575749056067	21743469	Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.	Ankylosing spondylitis	1	1	1	1
rs569805	9E-8	7.04575749056067	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	1	1	1
rs11206510	9E-8	7.04575749056067	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	1	1	1
rs9272535	9E-8	7.04575749056067	21131588	Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL.	Chronic lymphocytic leukemia	0	0	0	0
rs2444217	9E-8	7.04575749056067	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs12727642	9E-8	7.04575749056067	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs4333130	9E-8	7.04575749056067	20062062	Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.	Ankylosing spondylitis	0	0	1	1
rs7590268	9E-8	7.04575749056067	20023658	Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.	Orofacial clefts	0	0	1	1
rs13208776	9E-8	7.04575749056067	19890347	Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8.	Vitiligo	1	1	1	1
rs6426749	9E-8	7.04575749056067	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (hip)	0	0	0	0
rs987525	9E-8	7.04575749056067	19656524	A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.	Orofacial clefts	0	0	1	1
rs2104286	9E-8	7.04575749056067	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs17094273	9E-8	7.04575749056067	19340012	Genome-wide association study of tanning phenotype in a population of European ancestry.	Tanning	1	1	1	1
rs359312	9E-8	7.04575749056067	19176441	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.	Response to treatment for acute lymphoblastic leukemia	1	1	1	1
rs245201	9E-8	7.04575749056067	19023125	A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype.	Brain imaging in schizophrenia (interaction)	1	1	1	1
rs2542151	9E-8	7.04575749056067	18978792	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.	Type 1 diabetes	0	0	1	1
rs1678542	9E-8	7.04575749056067	18794853	Common variants at CD40 and other loci confer risk of rheumatoid arthritis.	Rheumatoid arthritis	0	1	1	1
rs501120	9E-8	7.04575749056067	17634449	Genomewide association analysis of coronary artery disease.	Coronary heart disease	0	0	1	1
rs8049439	1E-7	7	23722424	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.	Educational attainment	0	1	1	1
rs2017698	1E-7	7	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Se levels)	1	1	1	1
rs7148590	1E-7	7	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Zn levels)	0	1	1	1
rs17073641	1E-7	7	23577725	Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.	Age-related macular degeneration (smoking status interaction)	1	1	1	1
rs1379326	1E-7	7	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	1	1	1	1
rs267738	1E-7	7	23585552	Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.	Rhegmatogenous retinal detachment	0	1	1	1
rs1445130	1E-7	7	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs138206701	1E-7	7	23568457	Genetic variants associated with disordered eating.	Eating disorders (purging via substances) 	1	1	1	1
rs16923476	1E-7	7	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	1	1	1	1
rs10995190	1E-7	7	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	0	0	1	1
rs1243180	1E-7	7	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	0	0	0	0
rs7173419	1E-7	7	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Eye color	1	1	1	1
rs2290854	1E-7	7	23544013	Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.	Breast Cancer in BRCA1 mutation carriers	0	1	1	1
rs538867	1E-7	7	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs11688246	1E-7	7	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs4902141	1E-7	7	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs2859998	1E-7	7	23496005	Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study.	Narcolepsy with cataplexy	0	1	1	1
rs3117027	1E-7	7	23482656	Genome-wide association study of susceptibility loci for cervical cancer.	Cervical cancer	0	1	1	1
rs1662853	1E-7	7	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs2062377	1E-7	7	23437003	Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure.	Bone mineral density	0	0	0	0
rs9915657	1E-7	7	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs10504390	1E-7	7	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11619878	1E-7	7	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10995439	1E-7	7	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs5757676	1E-7	7	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1747683	1E-7	7	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs197273	1E-7	7	23372041	Novel locus including FGF21 is associated with dietary macronutrient intake.	Dietary macronutrient intake	0	1	1	1
rs12289961	1E-7	7	23349640	Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.	Lymphoma	0	0	0	0
rs2517388	1E-7	7	23307926	A genome-wide association study of early menopause and the combined impact of identified variants.	Menopause (age at onset)	0	0	1	1
rs963167	1E-7	7	23279374	Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain.	β2-Glycoprotein I (β2-GPI) plasma levels	1	1	1	1
rs4970988	1E-7	7	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs1035942	1E-7	7	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs635808	1E-7	7	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs1036429	1E-7	7	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs12716850   	1E-7	7	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs9368649   	1E-7	7	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs10007052	1E-7	7	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	1	1	1	1
rs1171113	1E-7	7	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	1	1	1	1
rs9834970	1E-7	7	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	0	1	1	1
rs10180496	1E-7	7	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs6472235	1E-7	7	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	0	1	1	1
rs2293579	1E-7	7	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	0	0	0	0
rs6936004	1E-7	7	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs3749982	1E-7	7	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs9469300	1E-7	7	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs10428959	1E-7	7	22890011	Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate.	Response to fenofibrate	1	1	1	1
rs2629751	1E-7	7	22841784	Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.	Hepatitis C induced liver fibrosis	0	1	1	1
rs2044029	1E-7	7	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	0	1	1	1
rs181654	1E-7	7	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs10454142	1E-7	7	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	1	1	1	1
rs9901675	1E-7	7	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	0	1	1
rs3794087	1E-7	7	22764253	Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor.	Essential tremor	0	1	1	1
rs4765905	1E-7	7	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	0	1	1	1
rs17154929	1E-7	7	22628157	Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults.	HIV-associated dementia 	1	1	1	1
rs542631	1E-7	7	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs5925760	1E-7	7	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	NA	NA	NA	NA
rs7060947	1E-7	7	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	NA	NA	NA	NA
rs17221323	1E-7	7	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs16970881	1E-7	7	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-10)	1	1	1	1
rs10055544	1E-7	7	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-10)	1	1	1	1
rs11845208	1E-7	7	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	NA	NA	NA	NA
rs17290760	1E-7	7	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune response to smallpox vaccine (IL-6)	1	1	1	1
rs1316952	1E-7	7	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	1	1	1
rs2241193	1E-7	7	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs10204325	1E-7	7	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (fairness)	1	1	1	1
rs2495478	1E-7	7	22544364	A genome-wide association study identifies susceptibility loci for Wilms tumor.	Wilms tumor	1	1	1	1
rs4607517	1E-7	7	22508271	Fasting glucose GWAS candidate region analysis across ethnic groups in the Multiethnic Study of Atherosclerosis (MESA).	Fasting plasma glucose	0	0	1	1
rs7852872	1E-7	7	22504421	Common variants at 12q14 and 12q24 are associated with hippocampal volume.	Hippocampal volume	0	1	1	1
rs13202860	1E-7	7	22509378	A genome-wide association study of female sexual dysfunction.	Sexual dysfunction (female)	1	1	1	1
rs7940423	1E-7	7	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs12109285	1E-7	7	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	NA	NA	NA	NA
rs16977065	1E-7	7	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs7006742	1E-7	7	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs4688011	1E-7	7	22354554	Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13.	Arthritis (juvenile idiopathic)	0	1	1	1
rs11216185	1E-7	7	22306654	Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis.	Infantile hypertrophic pyloric stenosis	0	1	1	1
rs8070463	1E-7	7	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	0	1	1	1
rs1801275	1E-7	7	22075330	A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study.	IgE levels 	1	1	1	1
rs228437	1E-7	7	21983787	Genome-wide association study identifies three new melanoma susceptibility loci.	Melanoma	1	1	1	1
rs12477314	1E-7	7	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	0	0	0
rs3094548	1E-7	7	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	1	1	1
rs4356203	1E-7	7	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	1	1	1
rs6511720	1E-7	7	21909108	Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.	Carotid intima media thickness	0	1	1	1
rs10861032	1E-7	7	21878436	A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary intervention.	Coronary restenosis	1	1	1	1
rs228614	1E-7	7	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs6062314	1E-7	7	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs3788013	1E-7	7	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	1	1	1
rs4939827	1E-7	7	21761138	Meta-analysis of new genome-wide association studies of colorectal cancer risk.	Colorectal cancer	0	0	1	1
rs11047102	1E-7	7	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	1	1	1	1
rs9275390	1E-7	7	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	0	0	0
rs7629490	1E-7	7	21743057	Genome-wide association study identifies new prostate cancer susceptibility loci.	Prostate cancer	0	0	1	1
rs823156	1E-7	7	21738487	Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.	Parkinson's disease	0	0	1	1
rs4803480	1E-7	7	21682944	DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population.	Schizophrenia	0	1	1	1
rs6852535	1E-7	7	21685912	Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.	Progressive supranuclear palsy	0	1	1	1
rs28675338	1E-7	7	21685187	Genome-wide association study of smoking behaviours in patients with COPD.	Chronic obstructive pulmonary disease	NA	NA	NA	NA
rs56238310	1E-7	7	21685187	Genome-wide association study of smoking behaviours in patients with COPD.	Chronic obstructive pulmonary disease	1	1	1	1
rs76884941	1E-7	7	21685187	Genome-wide association study of smoking behaviours in patients with COPD.	Chronic obstructive pulmonary disease	0	0	0	0
rs7157599	1E-7	7	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs5910578	1E-7	7	21623375	Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.	Paget's disease	NA	NA	NA	NA
rs9268905	1E-7	7	21602797	Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.	Cystic fibrosis severity	0	1	1	1
rs9512637	1E-7	7	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (heaviness of drinking)	1	1	1	1
rs1366594	1E-7	7	21533022	Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.	Bone mineral density	0	0	0	0
rs2698530	1E-7	7	21483845	Genome-wide association study identifies genetic loci associated with iron deficiency.	Iron status biomarkers	1	1	1	1
rs476141	1E-7	7	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs1061235	1E-7	7	21428769	HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans.	Adverse response to carbamapezine	0	1	1	1
rs2206277	1E-7	7	21386085	A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.	Metabolic syndrome (bivariate traits)	0	1	1	1
rs12757165	1E-7	7	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	1	1	1	1
rs16830359	1E-7	7	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	1	1	1	1
rs3734805	1E-7	7	21263130	Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study.	Breast cancer	0	0	1	1
rs12025416	1E-7	7	21244703	Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data.	Multiple sclerosis	0	0	1	1
rs2576037	1E-7	7	21173776	Meta-analysis of genome-wide association studies for personality.	Personality dimensions	0	1	1	1
rs11240594	1E-7	7	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Response to antipsychotic treatment	1	1	1	1
rs2687729	1E-7	7	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	0	1	1	1
rs2608053	1E-7	7	21037568	A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).	Hodgkin's lymphoma	1	1	1	1
rs11892031	1E-7	7	20972438	A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.	Bladder cancer	1	1	1	1
rs6809854	1E-7	7	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	0	1	1	1
rs1008953	1E-7	7	20953189	Genome-wide association analysis identifies three psoriasis susceptibility loci.	Psoriasis	1	1	1	1
rs1975974	1E-7	7	20953189	Genome-wide association analysis identifies three psoriasis susceptibility loci.	Psoriasis	1	1	1	1
rs867559	1E-7	7	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs1943816	1E-7	7	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	P-tau181p	1	1	1	1
rs2074955	1E-7	7	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	P-tau181p	1	1	1	1
rs7558386	1E-7	7	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	P-tau181p	1	1	1	1
rs10949808	1E-7	7	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs4996815	1E-7	7	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs225694	1E-7	7	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	1	1	1
rs2305480	1E-7	7	20860503	A large-scale, consortium-based genomewide association study of asthma.	Asthma	0	0	0	0
rs1295686	1E-7	7	20860503	A large-scale, consortium-based genomewide association study of asthma.	Asthma	0	1	1	1
rs11071559	1E-7	7	20860503	A large-scale, consortium-based genomewide association study of asthma.	Asthma	1	1	1	1
rs6859	1E-7	7	20885792	Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.	Alzheimer's disease (late onset)	0	1	1	1
rs2954021	1E-7	7	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	LDL cholesterol	0	0	0	0
rs2363956	1E-7	7	20852633	Common variants at 19p13 are associated with susceptibility to ovarian cancer.	Ovarian cancer	0	0	1	1
rs7903146	1E-7	7	20849430	The TCF7L2 diabetes risk variant is associated with HbA₁(C) levels: a genome-wide association meta-analysis.	Glycated hemoglobin levels	0	1	1	1
rs7890572	1E-7	7	20838585	Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.	Cardiovascular disease risk factors	NA	NA	NA	NA
rs9561329	1E-7	7	20634892	A genome-wide association study of neuroticism in a population-based sample.	Neuroticism	0	1	1	1
rs2188962	1E-7	7	20570966	Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.	Crohn's disease	0	0	1	1
rs2278729	1E-7	7	20548944	An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.	Osteoporosis	1	1	1	1
rs7044355	1E-7	7	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	1	1	1	1
rs7155603	1E-7	7	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	1	1	1	1
rs2476601	1E-7	7	20410501	Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.	Vitiligo	0	1	1	1
rs493258	1E-7	7	20385819	Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs1933182	1E-7	7	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs11959928	1E-7	7	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs4014195	1E-7	7	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	0	1	1	1
rs8067378	1E-7	7	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	0	0	0	0
rs6691768	1E-7	7	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	1	1	1	1
rs710865	1E-7	7	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs12243326	1E-7	7	20081857	Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.	Two-hour glucose challenge	0	1	1	1
rs17271305	1E-7	7	20081857	Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.	Two-hour glucose challenge	0	1	1	1
rs3825214	1E-7	7	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	0	0	0
rs12053903	1E-7	7	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	0	0	0
rs9367630	1E-7	7	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs2869967	1E-7	7	20010835	Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.	Pulmonary function	0	1	1	1
rs6532197	1E-7	7	19915575	Genome-wide association study reveals genetic risk underlying Parkinson's disease.	Parkinson's disease	0	0	1	1
rs6732426	1E-7	7	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	0	1	1	1
rs2227139	1E-7	7	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Hematological parameters	0	1	1	1
rs11856323	1E-7	7	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs5934953	1E-7	7	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	NA	NA	NA	NA
rs17390445	1E-7	7	19721433	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics.	Response to antipsychotic treatment	1	1	1	1
rs7543130	1E-7	7	19584346	Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.	Aortic root size	1	1	1	1
rs6782299	1E-7	7	19571811	Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.	Schizophrenia	1	1	1	1
rs17594526	1E-7	7	19571811	Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.	Schizophrenia	0	0	1	1
rs6074022	1E-7	7	19525955	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.	Multiple sclerosis	0	0	1	1
rs1335532	1E-7	7	19525955	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.	Multiple sclerosis	0	0	1	1
rs882300	1E-7	7	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	1	1	1	1
rs2151145	1E-7	7	19448619	Loci at chromosomes 13, 19 and 20 influence age at natural menopause.	Menopause (age at onset)	1	1	1	1
rs11258747	1E-7	7	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs448378	1E-7	7	19430479	Genome-wide association study of blood pressure and hypertension.	Systolic blood pressure	0	0	1	1
rs17418283	1E-7	7	19416921	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.	Bipolar disorder	1	1	1	1
rs16928809	1E-7	7	19414484	Genome-wide association meta-analysis for total serum bilirubin levels.	Bilirubin levels	1	1	1	1
rs910316	1E-7	7	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	1	1	1	1
rs1828591	1E-7	7	19300482	A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci.	Chronic obstructive pulmonary disease	0	1	1	1
rs10876432	1E-7	7	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (spine)	0	0	1	1
rs7138803	1E-7	7	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Body mass index	0	0	1	1
rs174546	1E-7	7	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	LDL cholesterol	0	0	1	1
rs10244051	1E-7	7	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	Metabolic traits	0	1	1	1
rs992037	1E-7	7	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	1	1	1	1
rs4775041	1E-7	7	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	0	0	1	1
rs6807064	1E-7	7	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	1	1	1	1
rs1591830	1E-7	7	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	1	1	1	1
rs17267292	1E-7	7	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	1	1	1	1
rs10983238	1E-7	7	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	0	1	1	1
rs220470	1E-7	7	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs7164335	1E-7	7	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs710521	1E-7	7	18794855	Sequence variant on 8q24 confers susceptibility to urinary bladder cancer.	Urinary bladder cancer	0	0	1	1
rs3890745	1E-7	7	18794853	Common variants at CD40 and other loci confer risk of rheumatoid arthritis.	Rheumatoid arthritis	0	1	1	1
rs11065611	1E-7	7	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs17369571	1E-7	7	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs3130340	1E-7	7	18445777	Multiple genetic loci for bone mineral density and fractures.	Bone mineral density (spine)	0	1	1	1
rs2075650	1E-7	7	18439552	Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein.	C-reactive protein	0	0	1	1
rs4794665	1E-7	7	18391951	Many sequence variants affecting diversity of adult human height.	Height	1	1	1	1
rs1016343	1E-7	7	18264097	Multiple newly identified loci associated with prostate cancer susceptibility.	Prostate cancer	0	0	1	1
rs10798269	1E-7	7	18204446	Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.	Systemic lupus erythematosus	1	1	1	1
rs255052	1E-7	7	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs599839	1E-7	7	18179892	Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.	LDL cholesterol	0	0	1	1
rs1121980	1E-7	7	18159244	Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants.	Obesity (early onset extreme)	0	0	1	1
rs6920220	1E-7	7	17982456	Two independent alleles at 6q23 associated with risk of rheumatoid arthritis.	Rheumatoid arthritis	0	0	0	0
rs1106683	1E-7	7	17903300	Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.	Body mass index	1	1	1	1
rs6599077	1E-7	7	17903308	Genome-wide association of sleep and circadian phenotypes.	Sleep duration	1	1	1	1
rs1379659	1E-7	7	17903301	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	Echocardiographic traits	1	1	1	1
rs2476601	1E-7	7	17632545	A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.	Type 1 diabetes	0	0	1	1
rs5219	1E-7	7	17463246	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	Type 2 diabetes	0	0	1	1
rs11227306	2E-7	6.69897000433602	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	0	1	1	1
rs2054125	2E-7	6.69897000433602	23722424	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.	Educational attainment	0	1	1	1
rs10740993	2E-7	6.69897000433602	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (time to first tooth eruption)	0	1	0	0
rs7005380	2E-7	6.69897000433602	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	1	1	1	1
rs11645781	2E-7	6.69897000433602	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs145241704	2E-7	6.69897000433602	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	1	1	1	1
rs17025867	2E-7	6.69897000433602	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	1	1	1	1
rs4141232	2E-7	6.69897000433602	23593202	Bivariate genome-wide association analyses identified genes with pleiotropic effects for femoral neck bone geometry and age at menarche.	Femoral neck bone geometry and menarche (age at onset)	1	1	1	1
rs2889829	2E-7	6.69897000433602	23555189	Genome-wide association study identifies genetic determinants of urine PCA3 levels in men.	PCA3 expression level	1	1	1	1
rs10818854	2E-7	6.69897000433602	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (non-asthmatics)	0	1	1	1
rs8170	2E-7	6.69897000433602	23535730	GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.	Ovarian cancer	0	0	0	0
rs12570744	2E-7	6.69897000433602	23555300	Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis.	Response to anti-TNF treatment in rheumatoid arthritis	1	1	1	1
rs340635	2E-7	6.69897000433602	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs1861525	2E-7	6.69897000433602	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs11252394	2E-7	6.69897000433602	23508266	A genome-wide association study of bronchodilator response in asthmatics.	Asthma (bronchodilator response)	1	1	1	1
rs12425451	2E-7	6.69897000433602	23496005	Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study.	Narcolepsy with cataplexy	1	1	1	1
rs17145638	2E-7	6.69897000433602	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Pit-and-Fissure caries 	NA	NA	NA	NA
rs6560397	2E-7	6.69897000433602	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Pit-and-Fissure caries 	0	1	1	1
rs11134654	2E-7	6.69897000433602	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Smooth-surface caries 	1	1	1	1
rs6907340	2E-7	6.69897000433602	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	0	0	1	1
rs2228467	2E-7	6.69897000433602	23314186	Genetic variation associated with circulating monocyte count in the eMERGE Network.	Monocyte count	1	1	1	1
rs1150668	2E-7	6.69897000433602	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs823094	2E-7	6.69897000433602	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs10980926	2E-7	6.69897000433602	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs11156429	2E-7	6.69897000433602	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	0	0	0
rs9275524	2E-7	6.69897000433602	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs11152369	2E-7	6.69897000433602	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs3132581	2E-7	6.69897000433602	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs12971120	2E-7	6.69897000433602	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	1	1	1	1
rs13015993	2E-7	6.69897000433602	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs9915657	2E-7	6.69897000433602	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs334699	2E-7	6.69897000433602	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs138880	2E-7	6.69897000433602	23894747	A comprehensive family-based replication study of schizophrenia genes.	Schizophrenia	1	1	1	1
rs2186369	2E-7	6.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs12600635	2E-7	6.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10861337	2E-7	6.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs17348299	2E-7	6.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1598106	2E-7	6.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10131728	2E-7	6.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2093746	2E-7	6.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs10504390	2E-7	6.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6421315	2E-7	6.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1747683	2E-7	6.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4917017	2E-7	6.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2072209	2E-7	6.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs603424 	2E-7	6.69897000433602	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitic acid (16:0) plasma levels	NA	NA	NA	NA
rs994988 	2E-7	6.69897000433602	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitic acid (16:0) plasma levels	NA	NA	NA	NA
rs3771395	2E-7	6.69897000433602	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs2830487	2E-7	6.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA)	1	1	1	1
rs2228638	2E-7	6.69897000433602	23297363	Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.	Tetralogy of Fallot	1	1	1	1
rs6449213	2E-7	6.69897000433602	23703922	A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls.	Uric acid levels	0	0	0	0
rs2168303	2E-7	6.69897000433602	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Gout	NA	NA	NA	NA
rs164009	2E-7	6.69897000433602	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs4777542	2E-7	6.69897000433602	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs4251631	2E-7	6.69897000433602	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs12477314	2E-7	6.69897000433602	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs2798641	2E-7	6.69897000433602	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs1928168   	2E-7	6.69897000433602	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs2078543   	2E-7	6.69897000433602	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs2544527   	2E-7	6.69897000433602	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs2456203   	2E-7	6.69897000433602	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs7780752	2E-7	6.69897000433602	23202124	New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.	Birth weight	1	1	1	1
rs6060373	2E-7	6.69897000433602	23207799	Genome-wide association study identified UQCC locus for spine bone size in humans.	Spine bone size	0	1	1	1
rs10500715	2E-7	6.69897000433602	23180869	Genome-wide association study of survival in patients with pancreatic adenocarcinoma.	Pancreatic cancer	0	1	1	1
rs6413458	2E-7	6.69897000433602	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity and mass	1	1	1	1
rs1429138	2E-7	6.69897000433602	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	0	1	1	1
rs6968355	2E-7	6.69897000433602	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs17103138	2E-7	6.69897000433602	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs7939886	2E-7	6.69897000433602	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	0	1	1	1
rs6843082	2E-7	6.69897000433602	23041239	Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.	Stroke (ischemic)	0	0	0	0
rs17079534	2E-7	6.69897000433602	23007406	Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs7588550	2E-7	6.69897000433602	23028342	New susceptibility loci associated with kidney disease in type 1 diabetes.	Type 1 diabetes nephropathy	1	1	1	1
rs10214886	2E-7	6.69897000433602	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs5001812	2E-7	6.69897000433602	22890011	Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate.	Response to fenofibrate	NA	NA	NA	NA
rs8076457	2E-7	6.69897000433602	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs17486278	2E-7	6.69897000433602	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	0	0	0	0
rs17496332	2E-7	6.69897000433602	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	0	0	0
rs13397985	2E-7	6.69897000433602	22700719	Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.	Chronic lymphocytic leukemia	0	0	1	1
rs4765905	2E-7	6.69897000433602	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	0	0	0	0
rs8127571	2E-7	6.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs4839431	2E-7	6.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs9807334	2E-7	6.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs10517025	2E-7	6.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs11034653	2E-7	6.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-12p40)	1	1	1	1
rs12542677	2E-7	6.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-1beta)	1	1	1	1
rs4963243	2E-7	6.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	0	1	1	1
rs758386	2E-7	6.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted TNF-alpha)	1	1	1	1
rs2501276	2E-7	6.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune response to smallpox vaccine (IL-6)	1	1	1	1
rs17299841	2E-7	6.69897000433602	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune response to smallpox vaccine (IL-6)	1	1	1	1
rs11041816	2E-7	6.69897000433602	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs308971	2E-7	6.69897000433602	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	0	1	1	1
rs1801282	2E-7	6.69897000433602	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	0	1	1	1
rs11643447	2E-7	6.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs7433808	2E-7	6.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	1	1	1
rs1898036	2E-7	6.69897000433602	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs4942242	2E-7	6.69897000433602	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs17118552	2E-7	6.69897000433602	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs1406428	2E-7	6.69897000433602	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs11937061	2E-7	6.69897000433602	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs800586	2E-7	6.69897000433602	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	0	1	1	1
rs4864201	2E-7	6.69897000433602	22484627	A genome-wide association meta-analysis identifies new childhood obesity loci.	Obesity	1	1	1	1
rs10794657	2E-7	6.69897000433602	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	1	1	1	1
rs1515110	2E-7	6.69897000433602	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	0	0	0
rs2108622	2E-7	6.69897000433602	22437554	Genome-wide association study identifies three common variants associated with serologic response to vitamin E supplementation in men.	Response to Vitamin E supplementation	0	1	1	1
rs11574514	2E-7	6.69897000433602	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	0	1	1	1
rs6430538	2E-7	6.69897000433602	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	0	1	1	1
rs6479891	2E-7	6.69897000433602	22354554	Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13.	Arthritis (juvenile idiopathic)	0	1	1	1
rs7769153	2E-7	6.69897000433602	22331829	Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial.	Response to statin therapy (LDL-C)	1	1	1	1
rs6728440	2E-7	6.69897000433602	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs702873	2E-7	6.69897000433602	22170493	Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL.	Psoriatic arthritis	0	0	0	0
rs10411936	2E-7	6.69897000433602	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	0	1	1	1
rs2681424	2E-7	6.69897000433602	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs7592330	2E-7	6.69897000433602	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs3102947	2E-7	6.69897000433602	22075330	A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study.	IgE levels 	1	1	1	1
rs10857636	2E-7	6.69897000433602	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	1	1	1	1
rs10517287	2E-7	6.69897000433602	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	1	1	1	1
rs11949289	2E-7	6.69897000433602	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	1	1	1	1
rs35390	2E-7	6.69897000433602	21983787	Genome-wide association study identifies three new melanoma susceptibility loci.	Melanoma	0	1	1	1
rs1928168	2E-7	6.69897000433602	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs2855812	2E-7	6.69897000433602	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	0	0	0
rs12716852	2E-7	6.69897000433602	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs4624519	2E-7	6.69897000433602	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	1	1	1
rs7004633	2E-7	6.69897000433602	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	0	1	1
rs10896135	2E-7	6.69897000433602	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	1	1	1	1
rs11953630	2E-7	6.69897000433602	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Hypertension	0	1	0	0
rs17608766	2E-7	6.69897000433602	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	0	0	0
rs12940887	2E-7	6.69897000433602	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs9727115	2E-7	6.69897000433602	21873549	Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.	Proinsulin levels	1	1	1	1
rs1520333	2E-7	6.69897000433602	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs7171171	2E-7	6.69897000433602	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	1	1	1
rs9983044	2E-7	6.69897000433602	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs1514178	2E-7	6.69897000433602	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs7435	2E-7	6.69897000433602	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs10488631	2E-7	6.69897000433602	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	0	0	0
rs4130047	2E-7	6.69897000433602	21738487	Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.	Parkinson's disease	0	0	1	1
rs6701037	2E-7	6.69897000433602	21703634	A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence.	Alcohol dependence	1	1	1	1
rs76351433	2E-7	6.69897000433602	21685187	Genome-wide association study of smoking behaviours in patients with COPD.	Chronic obstructive pulmonary disease	1	1	1	1
rs17126232	2E-7	6.69897000433602	21552555	A genome-wide association study on obesity and obesity-related traits.	Obesity	0	0	0	0
rs7581710	2E-7	6.69897000433602	21552555	A genome-wide association study on obesity and obesity-related traits.	Obesity	1	1	1	1
rs163030	2E-7	6.69897000433602	21502949	Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search.	Caudate nucleus volume	1	1	1	1
rs2698530	2E-7	6.69897000433602	21483845	Genome-wide association study identifies genetic loci associated with iron deficiency.	Iron status biomarkers	0	0	0	0
rs2819742	2E-7	6.69897000433602	21386754	Cerivastatin, genetic variants, and the risk of rhabdomyolysis.	Response to cerivastatin	1	1	1	1
rs62209	2E-7	6.69897000433602	21379329	Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE.	Alzheimer's disease (late onset)	1	1	1	1
rs2836878	2E-7	6.69897000433602	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	0	1	1	1
rs5771069	2E-7	6.69897000433602	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	0	1	1
rs10947055	2E-7	6.69897000433602	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	0	1	1	1
rs17636733	2E-7	6.69897000433602	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	NA	NA	NA	NA
rs6051520	2E-7	6.69897000433602	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs1862471	2E-7	6.69897000433602	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs12472911	2E-7	6.69897000433602	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs7554511	2E-7	6.69897000433602	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs4964469	2E-7	6.69897000433602	21084426	Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.	Parkinson's disease	1	1	1	1
rs2066808	2E-7	6.69897000433602	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	0	0	1	1
rs495337	2E-7	6.69897000433602	20953189	Genome-wide association analysis identifies three psoriasis susceptibility loci.	Psoriasis	0	0	1	1
rs1992045	2E-7	6.69897000433602	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs2509843	2E-7	6.69897000433602	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs802568	2E-7	6.69897000433602	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs10187066	2E-7	6.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	1	1	1	1
rs879882	2E-7	6.69897000433602	20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Height	0	0	1	1
rs2073643	2E-7	6.69897000433602	20860503	A large-scale, consortium-based genomewide association study of asthma.	Asthma	0	1	1	1
rs12449157	2E-7	6.69897000433602	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs6544366	2E-7	6.69897000433602	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs1227756	2E-7	6.69897000433602	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (lobular)	1	1	1	1
rs6498142	2E-7	6.69897000433602	20694011	Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.	Immunoglobulin A 	0	1	1	1
rs17043947	2E-7	6.69897000433602	20707712	A genome-wide association study of self-rated health.	Self-rated health	1	1	1	1
rs7016880	2E-7	6.69897000433602	20657596	Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.	Hypertriglyceridemia	0	1	1	1
rs4635554	2E-7	6.69897000433602	20657596	Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.	Hypertriglyceridemia	0	1	1	1
rs2503875	2E-7	6.69897000433602	20598377	Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs13081389	2E-7	6.69897000433602	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	0	1	1	1
rs776488	2E-7	6.69897000433602	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs7071247	2E-7	6.69897000433602	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	1	1	1	1
rs3761847	2E-7	6.69897000433602	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	0	1	1
rs215614	2E-7	6.69897000433602	20418888	Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior.	Smoking behavior	1	1	1	1
rs690037	2E-7	6.69897000433602	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (cup)	1	1	1	1
rs3858145	2E-7	6.69897000433602	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (cup)	0	1	0	0
rs6480314	2E-7	6.69897000433602	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (disc)	0	0	0	0
rs16864170	2E-7	6.69897000433602	20383146	New loci associated with kidney function and chronic kidney disease.	Chronic kidney disease	1	1	1	1
rs6570507	2E-7	6.69897000433602	20397748	Genome-wide association study of height and body mass index in Australian twin families.	Height	0	0	1	1
rs13390159	2E-7	6.69897000433602	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs1431005	2E-7	6.69897000433602	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs11584383	2E-7	6.69897000433602	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	0	0	1	1
rs1736135	2E-7	6.69897000433602	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	0	0	1	1
rs6806528	2E-7	6.69897000433602	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	1	1	1	1
rs6974491	2E-7	6.69897000433602	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs2298428	2E-7	6.69897000433602	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs13038095	2E-7	6.69897000433602	20173747	Common variants in KCNN3 are associated with lone atrial fibrillation.	Atrial fibrillation	1	1	1	1
rs234720	2E-7	6.69897000433602	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs17077540	2E-7	6.69897000433602	20125088	Genome-wide association study of recurrent early-onset major depressive disorder.	Major depressive disorder	1	1	1	1
rs4953911	2E-7	6.69897000433602	20117844	MGAT5 alters the severity of multiple sclerosis.	Multiple sclerosis (severity)	1	1	1	1
rs17324272	2E-7	6.69897000433602	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	NA	NA	NA	NA
rs6584283	2E-7	6.69897000433602	19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Ulcerative colitis	0	0	1	1
rs10048146	2E-7	6.69897000433602	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (hip)	0	1	0	0
rs6799705	2E-7	6.69897000433602	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs888219	2E-7	6.69897000433602	19721433	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics.	Response to antipsychotic treatment	1	1	1	1
rs10074258	2E-7	6.69897000433602	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs1888414	2E-7	6.69897000433602	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs139909	2E-7	6.69897000433602	19570815	A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.	Height	1	1	1	1
rs11865121	2E-7	6.69897000433602	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs6896969	2E-7	6.69897000433602	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs1497546	2E-7	6.69897000433602	19483685	HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin.	Drug-induced liver injury (flucloxacillin)	1	1	1	1
rs4699052	2E-7	6.69897000433602	19483681	A genome-wide association study of testicular germ cell tumor.	Testicular germ cell tumor	0	0	1	1
rs10488631	2E-7	6.69897000433602	19458352	Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.	Primary biliary cirrhosis	0	0	1	1
rs4843747	2E-7	6.69897000433602	19448619	Loci at chromosomes 13, 19 and 20 influence age at natural menopause.	Menopause (age at onset)	1	1	1	1
rs229541	2E-7	6.69897000433602	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	0	1	1
rs12444268	2E-7	6.69897000433602	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs16982520	2E-7	6.69897000433602	19430479	Genome-wide association study of blood pressure and hypertension.	Hypertension	0	0	1	1
rs472913	2E-7	6.69897000433602	19416921	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.	Bipolar disorder	1	1	1	1
rs1042779	2E-7	6.69897000433602	19416921	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.	Bipolar disorder	0	1	1	1
rs999737	2E-7	6.69897000433602	19330030	A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).	Breast cancer	0	0	1	1
rs6437740	2E-7	6.69897000433602	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	1	1	1	1
rs10508503	2E-7	6.69897000433602	19151714	Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.	Obesity	1	1	1	1
rs2573905	2E-7	6.69897000433602	19136949	Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease.	Alzheimer's disease	NA	NA	NA	NA
rs6749447	2E-7	6.69897000433602	19114657	From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.	Blood pressure	0	1	1	1
rs6265	2E-7	6.69897000433602	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	0	0	0
rs7138803	2E-7	6.69897000433602	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	1	0	0
rs9891572	2E-7	6.69897000433602	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	HDL cholesterol	1	1	1	1
rs4844614	2E-7	6.69897000433602	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	LDL cholesterol	0	1	1	1
rs5031002	2E-7	6.69897000433602	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	LDL cholesterol	NA	NA	NA	NA
rs11668477	2E-7	6.69897000433602	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	LDL cholesterol	0	0	1	1
rs11790994	2E-7	6.69897000433602	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	1	1	1	1
rs10517480	2E-7	6.69897000433602	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	1	1	1	1
rs10953730	2E-7	6.69897000433602	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	1	1	1	1
rs886144	2E-7	6.69897000433602	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	1	1	1	1
rs1344706	2E-7	6.69897000433602	18677311	Identification of loci associated with schizophrenia by genome-wide association and follow-up.	Schizophrenia	1	1	1	1
rs6028945	2E-7	6.69897000433602	18615156	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.	Response to TNF antagonist treatment	1	1	1	1
rs5751901	2E-7	6.69897000433602	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	1	1	1
rs4950322	2E-7	6.69897000433602	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs9635963	2E-7	6.69897000433602	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs4870044	2E-7	6.69897000433602	18445777	Multiple genetic loci for bone mineral density and fractures.	Bone mineral density (hip)	0	0	0	0
rs946053	2E-7	6.69897000433602	18391951	Many sequence variants affecting diversity of adult human height.	Height	1	1	1	1
rs3825199	2E-7	6.69897000433602	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs1153188	2E-7	6.69897000433602	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	1	1	1	1
rs17036101	2E-7	6.69897000433602	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs7020996	2E-7	6.69897000433602	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs4962416	2E-7	6.69897000433602	18264096	Multiple loci identified in a genome-wide association study of prostate cancer.	Prostate cancer	1	1	1	1
rs2156552	2E-7	6.69897000433602	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	HDL cholesterol	0	0	1	1
rs693	2E-7	6.69897000433602	18193044	Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.	Triglycerides	0	0	0	0
rs4471028	2E-7	6.69897000433602	17903300	Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.	Waist circumference	1	1	1	1
rs9317284	2E-7	6.69897000433602	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Bone mineral density	NA	NA	NA	NA
rs10514345	2E-7	6.69897000433602	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	1	1	1	1
rs10506821	2E-7	6.69897000433602	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	1	1	1	1
rs10503887	2E-7	6.69897000433602	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	1	1	1	1
rs2548003	2E-7	6.69897000433602	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	1	1	1	1
rs3773643	2E-7	6.69897000433602	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Tonometry	1	1	1	1
rs4133289	2E-7	6.69897000433602	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	0	1	1	1
rs7159841	2E-7	6.69897000433602	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs2943634	2E-7	6.69897000433602	17634449	Genomewide association analysis of coronary artery disease.	Coronary heart disease	0	1	1	1
rs17228212	2E-7	6.69897000433602	17634449	Genomewide association analysis of coronary artery disease.	Coronary heart disease	0	1	1	1
rs2542151	2E-7	6.69897000433602	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Crohn's disease	0	0	1	1
rs9939609	2E-7	6.69897000433602	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 2 diabetes	0	0	1	1
rs12035082	2E-7	6.69897000433602	17554261	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.	Crohn's disease	0	0	1	1
rs3741208	2E-7	6.69897000433602	17554260	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.	Type 1 diabetes	0	0	1	1
rs3227	3E-7	6.52287874528034	23722424	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.	Educational attainment	0	1	1	1
rs1458303	3E-7	6.52287874528034	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Cu levels)	1	1	1	1
rs1395479	3E-7	6.52287874528034	23698163	Genome-wide association study of serum selenium concentrations.	Serum selenium levels	1	1	1	1
rs210138	3E-7	6.52287874528034	23666239	Meta-analysis identifies four new loci associated with testicular germ cell tumor.	Testicular germ cell tumor	0	0	1	1
rs522162	3E-7	6.52287874528034	23577725	Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.	Age-related macular degeneration (extreme sampling)	0	1	0	0
rs838145	3E-7	6.52287874528034	23636237	Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake.	Dietary macronutrient intake	0	0	0	0
rs7722600	3E-7	6.52287874528034	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs13413635	3E-7	6.52287874528034	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	0	1	1	1
rs62090893	3E-7	6.52287874528034	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	1	1	1	1
rs3782724	3E-7	6.52287874528034	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	1	1	1	1
rs12896399	3E-7	6.52287874528034	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Eye color	0	0	0	0
rs147845115	3E-7	6.52287874528034	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs74006954	3E-7	6.52287874528034	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs12565140	3E-7	6.52287874528034	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs12118390	3E-7	6.52287874528034	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs9283487	3E-7	6.52287874528034	23472185	Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.	Multiple sclerosis (OCB status)	NA	NA	NA	NA
rs9568281	3E-7	6.52287874528034	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs733724	3E-7	6.52287874528034	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs11755845 	3E-7	6.52287874528034	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	NA	NA	NA	NA
rs17723470	3E-7	6.52287874528034	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs589249	3E-7	6.52287874528034	23894747	A comprehensive family-based replication study of schizophrenia genes.	Schizophrenia	1	1	1	1
rs3132935	3E-7	6.52287874528034	23894747	A comprehensive family-based replication study of schizophrenia genes.	Schizophrenia	0	0	1	1
rs7897654	3E-7	6.52287874528034	23894747	A comprehensive family-based replication study of schizophrenia genes.	Schizophrenia	0	0	1	1
rs2546057	3E-7	6.52287874528034	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	0	1	1	1
rs7174755	3E-7	6.52287874528034	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs4585146	3E-7	6.52287874528034	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs4720952	3E-7	6.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7529251	3E-7	6.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4711279	3E-7	6.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6072161	3E-7	6.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2659005	3E-7	6.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2093746	3E-7	6.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs1794265	3E-7	6.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs459482	3E-7	6.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11665307	3E-7	6.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1747683	3E-7	6.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs300032	3E-7	6.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs12529874 	3E-7	6.52287874528034	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Oleic acid (18:1n-9) plasma levels	NA	NA	NA	NA
rs2366017 	3E-7	6.52287874528034	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	NA	NA	NA	NA
rs742614 	3E-7	6.52287874528034	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Stearic acid (18:0) plasma levels	NA	NA	NA	NA
rs948562	3E-7	6.52287874528034	23349640	Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.	Lymphoma	0	0	0	0
rs1473307	3E-7	6.52287874528034	23307926	A genome-wide association study of early menopause and the combined impact of identified variants.	Menopause (age at onset)	1	1	1	1
rs2647528	3E-7	6.52287874528034	23279374	Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain.	β2-Glycoprotein I (β2-GPI) plasma levels	0	0	0	0
rs3217901	3E-7	6.52287874528034	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	1	1	1	1
rs13130787	3E-7	6.52287874528034	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	1	1	1	1
rs1383934	3E-7	6.52287874528034	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	0	1	1	1
rs8089099   	3E-7	6.52287874528034	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs10751226   	3E-7	6.52287874528034	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs7233060	3E-7	6.52287874528034	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	1	1	1	1
rs7583877	3E-7	6.52287874528034	23028342	New susceptibility loci associated with kidney disease in type 1 diabetes.	Type 1 diabetes nephropathy	0	0	0	0
rs10046257	3E-7	6.52287874528034	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs17530068	3E-7	6.52287874528034	22976474	A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.	Breast cancer	0	0	1	1
rs7477	3E-7	6.52287874528034	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	1	1	1	1
rs39861	3E-7	6.52287874528034	22949513	Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32	Epilepsy (generalized)	1	1	1	1
rs2834215	3E-7	6.52287874528034	22936669	A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.	Crohn's disease	0	0	1	1
rs41350144	3E-7	6.52287874528034	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	0	1	1	1
rs9285640	3E-7	6.52287874528034	22890011	Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate.	Response to fenofibrate	1	1	1	1
rs4150167	3E-7	6.52287874528034	22843504	Individual common variants exert weak effects on the risk for autism spectrum disorderspi.	Autism	1	1	1	1
rs16965962	3E-7	6.52287874528034	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	NA	NA	NA	NA
rs11800854	3E-7	6.52287874528034	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	1	1	1	1
rs2842992	3E-7	6.52287874528034	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (GA)	1	1	1	1
rs17746001	3E-7	6.52287874528034	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder	1	1	1	1
rs17746001	3E-7	6.52287874528034	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder and schizophrenia	0	1	0	0
rs12592967	3E-7	6.52287874528034	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	1	1	1	1
rs10894294	3E-7	6.52287874528034	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	1	1	1	1
rs404005	3E-7	6.52287874528034	22628157	Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults.	HIV-associated dementia 	1	1	1	1
rs261532	3E-7	6.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	0	0	0	0
rs17714988	3E-7	6.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs6679454	3E-7	6.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-10)	1	1	1	1
rs3736638	3E-7	6.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-12p40)	1	1	1	1
rs859267	3E-7	6.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-12p40)	1	1	1	1
rs6943090	3E-7	6.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-12p40)	NA	NA	NA	NA
rs902464	3E-7	6.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-1beta)	1	1	1	1
rs4827947	3E-7	6.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-1beta)	NA	NA	NA	NA
rs1473500	3E-7	6.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	1	1	1	1
rs2255327	3E-7	6.52287874528034	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune response to smallpox vaccine (IL-6)	NA	NA	NA	NA
rs3748140	3E-7	6.52287874528034	22832961	Genome-wide association study of Alzheimer's disease.	Alzheimer's disease	1	1	1	1
rs17608059	3E-7	6.52287874528034	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	1	1	1	1
rs2714337	3E-7	6.52287874528034	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs2040862	3E-7	6.52287874528034	22544366	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	Atrial fibrillation	0	1	1	1
rs6741949	3E-7	6.52287874528034	22504421	Common variants at 12q14 and 12q24 are associated with hippocampal volume.	Hippocampal volume	1	1	1	1
rs6138892	3E-7	6.52287874528034	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs1809529	3E-7	6.52287874528034	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs1543922	3E-7	6.52287874528034	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs4698412	3E-7	6.52287874528034	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	0	0	1	1
rs10995170	3E-7	6.52287874528034	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	0	1	1	1
rs12411988	3E-7	6.52287874528034	22354554	Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13.	Arthritis (juvenile idiopathic)	0	0	0	0
rs931608	3E-7	6.52287874528034	22331829	Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial.	Response to statin therapy (LDL-C)	1	1	1	1
rs12532960	3E-7	6.52287874528034	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs3764563	3E-7	6.52287874528034	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs12722605	3E-7	6.52287874528034	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	0	0	0	0
rs1413885	3E-7	6.52287874528034	22216198	A genome-wide association study of the Protein C anticoagulant pathway.	Anticoagulant levels	1	1	1	1
rs13141641	3E-7	6.52287874528034	22080838	A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13.	Chronic obstructive pulmonary disease	0	0	1	1
rs7136572	3E-7	6.52287874528034	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	1	1	1	1
rs17766217	3E-7	6.52287874528034	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	1	1	1	1
rs10994397	3E-7	6.52287874528034	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	0	0	1	1
rs2932538	3E-7	6.52287874528034	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Hypertension	0	1	0	0
rs13139571	3E-7	6.52287874528034	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs630923	3E-7	6.52287874528034	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs183211	3E-7	6.52287874528034	21812969	Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.	Parkinson's disease	0	0	1	1
rs2844665	3E-7	6.52287874528034	21801394	Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.	Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS-TEN)	0	0	0	0
rs3815087	3E-7	6.52287874528034	21801394	Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.	Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS-TEN)	0	0	0	0
rs16832011	3E-7	6.52287874528034	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs4985167	3E-7	6.52287874528034	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	1	1
rs7698623	3E-7	6.52287874528034	21779381	Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study.	Cardiovascular disease risk factors	0	1	1	1
rs10440635	3E-7	6.52287874528034	21743469	Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.	Ankylosing spondylitis	0	1	1	1
rs2179367	3E-7	6.52287874528034	21732829	Wnt signaling and Dupuytren's disease.	Dupuytren's disease	1	1	1	1
rs2142991	3E-7	6.52287874528034	21685912	Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.	Progressive supranuclear palsy	1	1	1	1
rs10928927	3E-7	6.52287874528034	21685187	Genome-wide association study of smoking behaviours in patients with COPD.	Chronic obstructive pulmonary disease	1	1	1	1
rs73717741	3E-7	6.52287874528034	21685187	Genome-wide association study of smoking behaviours in patients with COPD.	Chronic obstructive pulmonary disease	1	1	1	1
rs12155623	3E-7	6.52287874528034	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs17291650	3E-7	6.52287874528034	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs1558477	3E-7	6.52287874528034	21621269	Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples.	Major depressive disorder	1	1	1	1
rs2807278	3E-7	6.52287874528034	21552555	A genome-wide association study on obesity and obesity-related traits.	Obesity	1	1	1	1
rs8040009	3E-7	6.52287874528034	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (heaviness of drinking)	1	1	1	1
rs6693017	3E-7	6.52287874528034	21493818	Genetic and clinical correlates of early-outgrowth colony-forming units.	Monocyte early outgrowth colony forming units	0	1	1	1
rs2472304	3E-7	6.52287874528034	21490707	Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.	Caffeine consumption	0	0	0	0
rs6028466	3E-7	6.52287874528034	21460395	A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer.	Telomere length	1	1	1	1
rs1789924	3E-7	6.52287874528034	21437268	A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium.	Upper aerodigestive tract cancers	0	1	1	1
rs2736340	3E-7	6.52287874528034	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	0	0	1	1
rs1020388	3E-7	6.52287874528034	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	1	1	1	1
rs2738113	3E-7	6.52287874528034	21151130	Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis.	Endometriosis	1	1	1	1
rs749005	3E-7	6.52287874528034	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	MRI atrophy measures	1	1	1	1
rs1569476	3E-7	6.52287874528034	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	0	1	1	1
rs3914188	3E-7	6.52287874528034	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	0	1	1	1
rs2243803	3E-7	6.52287874528034	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs2075650	3E-7	6.52287874528034	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	AB1-42	0	1	1	1
rs10784496	3E-7	6.52287874528034	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	AB1-42	1	1	1	1
rs17189298	3E-7	6.52287874528034	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	T-tau	1	1	1	1
rs2665390	3E-7	6.52287874528034	20852632	A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.	Ovarian cancer	0	0	1	1
rs4561213	3E-7	6.52287874528034	20700443	Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.	Magnesium levels	1	1	1	1
rs9491140	3E-7	6.52287874528034	20634892	A genome-wide association study of neuroticism in a population-based sample.	Neuroticism	1	1	1	1
rs11013962	3E-7	6.52287874528034	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs2239557	3E-7	6.52287874528034	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs3750965	3E-7	6.52287874528034	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Hair color	0	1	1	1
rs2159128	3E-7	6.52287874528034	20548946	A genome-wide association study of optic disc parameters.	Vertical cup-disc ratio	NA	NA	NA	NA
rs346291	3E-7	6.52287874528034	20522523	Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.	Partial epilepsies	1	1	1	1
rs7574865	3E-7	6.52287874528034	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs12638540	3E-7	6.52287874528034	20400778	Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.	Mortality among heart failure patients	1	1	1	1
rs1192415	3E-7	6.52287874528034	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (disc)	0	1	1	1
rs491391	3E-7	6.52287874528034	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (disc)	1	1	1	1
rs2285714	3E-7	6.52287874528034	20385819	Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs3791675	3E-7	6.52287874528034	20397748	Genome-wide association study of height and body mass index in Australian twin families.	Height	0	0	1	1
rs2456930	3E-7	6.52287874528034	20197096	Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.	Brain structure (temporal lobe volume)	1	1	1	1
rs17122693	3E-7	6.52287874528034	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs2244012	3E-7	6.52287874528034	20159242	Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions.	Asthma	0	0	1	1
rs259919	3E-7	6.52287874528034	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	0	1	1	1
rs16914280	3E-7	6.52287874528034	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	NA	NA	NA	NA
rs9574565	3E-7	6.52287874528034	20023658	Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.	Orofacial clefts	0	0	1	1
rs7524102	3E-7	6.52287874528034	19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Ulcerative colitis	0	0	1	1
rs9548988	3E-7	6.52287874528034	19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Ulcerative colitis	1	1	1	1
rs1840440	3E-7	6.52287874528034	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Weight	1	1	1	1
rs1473247	3E-7	6.52287874528034	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	0	0	1	1
rs1206397	3E-7	6.52287874528034	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs2203512	3E-7	6.52287874528034	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs2326017	3E-7	6.52287874528034	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	0	1	1	1
rs767210	3E-7	6.52287874528034	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs7968606	3E-7	6.52287874528034	19721433	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics.	Response to antipsychotic treatment	NA	NA	NA	NA
rs2239633	3E-7	6.52287874528034	19684604	Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs11155133	3E-7	6.52287874528034	19684603	Germline genomic variants associated with childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs3790268	3E-7	6.52287874528034	20031604	Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels.	Matrix metalloproteinase levels	1	1	1	1
rs12767583	3E-7	6.52287874528034	19578179	A genome-wide association study of acenocoumarol maintenance dosage.	Acenocoumarol maintenance dosage	0	0	0	0
rs10472828	3E-7	6.52287874528034	19570815	A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.	Height	0	0	1	1
rs2312147	3E-7	6.52287874528034	19571808	Common variants conferring risk of schizophrenia.	Schizophrenia	0	1	1	1
rs6429082	3E-7	6.52287874528034	19557161	Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.	Adiposity	1	1	1	1
rs4397868	3E-7	6.52287874528034	19448619	Loci at chromosomes 13, 19 and 20 influence age at natural menopause.	Menopause (age at onset)	1	1	1	1
rs6468442	3E-7	6.52287874528034	19448619	Loci at chromosomes 13, 19 and 20 influence age at natural menopause.	Menopause (age at onset)	1	1	1	1
rs10472828	3E-7	6.52287874528034	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs1805081	3E-7	6.52287874528034	19151714	Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.	Obesity	1	1	1	1
rs11610206	3E-7	6.52287874528034	19118814	Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease.	Alzheimer's disease	1	1	1	1
rs2274089	3E-7	6.52287874528034	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	0	1	1
rs10889353	3E-7	6.52287874528034	19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	Triglycerides	0	0	1	1
rs11185790	3E-7	6.52287874528034	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	Metabolic traits	1	1	1	1
rs806276	3E-7	6.52287874528034	18937294	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.	Attention deficit hyperactivity disorder (time to onset)	1	1	1	1
rs9354308	3E-7	6.52287874528034	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	1	1	1	1
rs2194980	3E-7	6.52287874528034	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	1	1	1	1
rs2587695	3E-7	6.52287874528034	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs10945919	3E-7	6.52287874528034	18615156	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.	Response to TNF antagonist treatment	1	1	1	1
rs6761	3E-7	6.52287874528034	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	1	1	1
rs6455128	3E-7	6.52287874528034	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs2730245	3E-7	6.52287874528034	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	1	1	1	1
rs8099594	3E-7	6.52287874528034	18391952	Genome-wide association analysis identifies 20 loci that influence adult height.	Height	0	0	1	1
rs6441961	3E-7	6.52287874528034	18311140	Newly identified genetic risk variants for celiac disease related to the immune response.	Celiac disease	0	0	1	1
rs4087296	3E-7	6.52287874528034	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Bone mineral density	1	1	1	1
rs7591163	3E-7	6.52287874528034	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Blood pressure	1	1	1	1
rs10496262	3E-7	6.52287874528034	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Aging traits	0	0	0	0
rs882300	3E-7	6.52287874528034	17903306	Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.	Electrocardiographic traits	0	1	1	1
rs6897932	3E-7	6.52287874528034	17660530	Risk alleles for multiple sclerosis identified by a genomewide study.	Multiple sclerosis	0	0	1	1
rs1000113	3E-7	6.52287874528034	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Crohn's disease	0	0	1	1
rs9465871	3E-7	6.52287874528034	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 2 diabetes	0	0	1	1
rs891684	4E-7	6.39794000867204	23698163	Genome-wide association study of serum selenium concentrations.	Serum selenium levels	1	1	1	1
rs755383	4E-7	6.39794000867204	23666239	Meta-analysis identifies four new loci associated with testicular germ cell tumor.	Testicular germ cell tumor	0	0	1	1
rs10515808	4E-7	6.39794000867204	23643386	Weight loss after gastric bypass is associated with a variant at 15q26.1.	Weight loss (gastric bypass surgery)	1	1	1	1
rs58667	4E-7	6.39794000867204	23541324	Genome-wide association study identifies TH1 pathway genes associated with lung function in asthmatic patients.	Pulmonary function in asthmatics	1	1	1	1
rs146579248	4E-7	6.39794000867204	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs1399439	4E-7	6.39794000867204	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs9934540	4E-7	6.39794000867204	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs10508881	4E-7	6.39794000867204	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	0	1	1	1
rs2521634	4E-7	6.39794000867204	23459936	Exploring the genetic basis of chronic periodontitis: a genome-wide association study.	Periodontitis	1	1	1	1
rs9297357	4E-7	6.39794000867204	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs11726248	4E-7	6.39794000867204	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs16897515	4E-7	6.39794000867204	23894747	A comprehensive family-based replication study of schizophrenia genes.	Schizophrenia	0	0	1	1
rs12410462	4E-7	6.39794000867204	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs17538444	4E-7	6.39794000867204	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs9403856	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs2200578	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7111562	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2659005	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7652995	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2279913	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6687262	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs12600635	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11711311	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11568995	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7209700	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs1470506	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11260603	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1747683	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4720952	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10813951	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs3813009	4E-7	6.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4465599 	4E-7	6.39794000867204	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	NA	NA	NA	NA
rs2118674	4E-7	6.39794000867204	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	1	1	1	1
rs12098564 	4E-7	6.39794000867204	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Stearic acid (18:0) plasma levels	NA	NA	NA	NA
rs4766646	4E-7	6.39794000867204	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs10813960	4E-7	6.39794000867204	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs3802842	4E-7	6.39794000867204	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	0	0	1	1
rs59336	4E-7	6.39794000867204	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	0	1	1	1
rs17057381	4E-7	6.39794000867204	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs8089099   	4E-7	6.39794000867204	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs10751226   	4E-7	6.39794000867204	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs2027760   	4E-7	6.39794000867204	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs3003429   	4E-7	6.39794000867204	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs3734729   	4E-7	6.39794000867204	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs2252711   	4E-7	6.39794000867204	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs11704416	4E-7	6.39794000867204	23065704	A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease.	Prostate cancer	0	1	1	1
rs4683505	4E-7	6.39794000867204	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs9505270	4E-7	6.39794000867204	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs569688	4E-7	6.39794000867204	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs2084898	4E-7	6.39794000867204	22990015	A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke.	Stroke (pediatric)	1	1	1	1
rs4875102	4E-7	6.39794000867204	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs2444240	4E-7	6.39794000867204	22969067	Genetic variants near PDGFRA are associated with corneal curvature in Australians.	Corneal curvature	0	1	1	1
rs3849942	4E-7	6.39794000867204	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	0	0	1	1
rs2717068	4E-7	6.39794000867204	22949513	Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32	Epilepsy (generalized)	0	0	0	0
rs4675502	4E-7	6.39794000867204	22843504	Individual common variants exert weak effects on the risk for autism spectrum disorderspi.	Autism	1	1	1	1
rs12905014	4E-7	6.39794000867204	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs17281398	4E-7	6.39794000867204	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	NA	NA	NA	NA
rs4820792	4E-7	6.39794000867204	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs9349379	4E-7	6.39794000867204	22745674	Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis.	Coronary heart disease	0	0	0	0
rs1789110	4E-7	6.39794000867204	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (GA)	1	1	1	1
rs1783925	4E-7	6.39794000867204	22648509	PKNOX2 is associated with formal thought disorder in schizophrenia: a meta-analysis of two genome-wide association studies.	Formal thought disorder in schizophrenia	1	1	1	1
rs9493873	4E-7	6.39794000867204	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs9883650	4E-7	6.39794000867204	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-1beta)	1	1	1	1
rs10513432	4E-7	6.39794000867204	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	1	1	1	1
rs1372791	4E-7	6.39794000867204	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	1	1	1	1
rs1392089	4E-7	6.39794000867204	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	1	1	1	1
rs7224438	4E-7	6.39794000867204	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	1	1	1	1
rs11889798	4E-7	6.39794000867204	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted TNF-alpha)	1	1	1	1
rs1791780	4E-7	6.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs10937540	4E-7	6.39794000867204	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	1	1	1	1
rs11233413	4E-7	6.39794000867204	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (feminism/equality)	1	1	1	1
rs16938910	4E-7	6.39794000867204	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	NA	NA	NA	NA
rs592423	4E-7	6.39794000867204	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	1	1	1
rs964184	4E-7	6.39794000867204	22437554	Genome-wide association study identifies three common variants associated with serologic response to vitamin E supplementation in men.	Response to Vitamin E supplementation	0	0	0	0
rs11865038	4E-7	6.39794000867204	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	0	1	1	1
rs2746347	4E-7	6.39794000867204	22286170	The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes.	Lymphocyte counts	1	1	1	1
rs13241427	4E-7	6.39794000867204	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	1	1	1	1
rs1738074	4E-7	6.39794000867204	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs1250542	4E-7	6.39794000867204	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs6746082	4E-7	6.39794000867204	22120009	Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.	Multiple myeloma	1	1	1	1
rs17647114	4E-7	6.39794000867204	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	1	1	1	1
rs6724422	4E-7	6.39794000867204	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	0	0	0	0
rs527430	4E-7	6.39794000867204	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	1	1	1	1
rs1000579	4E-7	6.39794000867204	22004471	Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.	Alcohol dependence	1	1	1	1
rs12679857	4E-7	6.39794000867204	21980299	A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.	Type 1 diabetes	0	1	1	1
rs17045031	4E-7	6.39794000867204	21909108	Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.	Carotid intima media thickness	1	1	1	1
rs7129220	4E-7	6.39794000867204	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs9586179	4E-7	6.39794000867204	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs16892766	4E-7	6.39794000867204	21761138	Meta-analysis of new genome-wide association studies of colorectal cancer risk.	Colorectal cancer	0	0	1	1
rs3802842	4E-7	6.39794000867204	21761138	Meta-analysis of new genome-wide association studies of colorectal cancer risk.	Colorectal cancer	0	0	1	1
rs2143678	4E-7	6.39794000867204	21779381	Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study.	Cardiovascular disease risk factors	1	1	1	1
rs10488631	4E-7	6.39794000867204	21750679	Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.	Systemic sclerosis	0	0	1	1
rs117607728	4E-7	6.39794000867204	21685187	Genome-wide association study of smoking behaviours in patients with COPD.	Chronic obstructive pulmonary disease	1	1	1	1
rs950776	4E-7	6.39794000867204	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	0	1	1	1
rs2251393	4E-7	6.39794000867204	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs2389202	4E-7	6.39794000867204	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs10829156	4E-7	6.39794000867204	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs11187837	4E-7	6.39794000867204	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	0	1	1	1
rs17126232	4E-7	6.39794000867204	21552555	A genome-wide association study on obesity and obesity-related traits.	Obesity	0	0	0	0
rs285480	4E-7	6.39794000867204	21368711	Genome-wide association study of personality traits in bipolar patients.	Personality dimensions	0	1	1	1
rs6777876	4E-7	6.39794000867204	21314694	Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.	Alcohol dependence	1	1	1	1
rs931555	4E-7	6.39794000867204	21244703	Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data.	Multiple sclerosis	0	0	1	1
rs7780564	4E-7	6.39794000867204	21216879	A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3.	Insulin-like growth factors	1	1	1	1
rs2208059	4E-7	6.39794000867204	21139019	A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum.	Ileal carcinoids	1	1	1	1
rs11110077	4E-7	6.39794000867204	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Working memory	1	1	1	1
rs7065696	4E-7	6.39794000867204	21057379	Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes.	Bipolar disorder and schizophrenia	NA	NA	NA	NA
rs7824557	4E-7	6.39794000867204	21060863	Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo.	Retinal vascular caliber	0	1	1	1
rs2076529	4E-7	6.39794000867204	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	0	1	1	1
rs3764400	4E-7	6.39794000867204	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs4949526	4E-7	6.39794000867204	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs6046396	4E-7	6.39794000867204	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs3803662	4E-7	6.39794000867204	20872241	A combined analysis of genome-wide association studies in breast cancer.	Breast cancer	0	0	1	1
rs11902417	4E-7	6.39794000867204	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	HDL cholesterol	0	0	0	0
rs958798	4E-7	6.39794000867204	20707712	A genome-wide association study of self-rated health.	Self-rated health	NA	NA	NA	NA
rs10760706	4E-7	6.39794000867204	20596022	Genome-wide association study in alopecia areata implicates both innate and adaptive immunity.	Alopecia areata	1	1	1	1
rs694739	4E-7	6.39794000867204	20596022	Genome-wide association study in alopecia areata implicates both innate and adaptive immunity.	Alopecia areata	0	1	1	1
rs4958351	4E-7	6.39794000867204	20592726	Genetic variations in GRIA1 on chromosome 5q33 related to asparaginase hypersensitivity.	Asparaginase hypersensitivity in acute lymphoblastic leukemia	0	1	1	1
rs1535480	4E-7	6.39794000867204	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs4935969	4E-7	6.39794000867204	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Hair color	0	1	1	1
rs12203592	4E-7	6.39794000867204	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Hair color	0	0	0	0
rs7227401	4E-7	6.39794000867204	20548944	An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.	Osteoporosis	1	1	1	1
rs12131057	4E-7	6.39794000867204	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	1	1	1	1
rs6611365	4E-7	6.39794000867204	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (disc)	NA	NA	NA	NA
rs2275215	4E-7	6.39794000867204	20397748	Genome-wide association study of height and body mass index in Australian twin families.	Body mass index	1	1	1	1
rs8756	4E-7	6.39794000867204	20397748	Genome-wide association study of height and body mass index in Australian twin families.	Height	0	0	1	1
rs7183263	4E-7	6.39794000867204	20397748	Genome-wide association study of height and body mass index in Australian twin families.	Height	0	0	1	1
rs2136093	4E-7	6.39794000867204	20360315	Genome-wide pharmacogenetics of antidepressant response in the GENDEP project.	Response to antidepressants	1	1	1	1
rs6799767	4E-7	6.39794000867204	20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Eosinophilic esophagitis (pediatric)	1	1	1	1
rs864537	4E-7	6.39794000867204	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs4899260	4E-7	6.39794000867204	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs6435957	4E-7	6.39794000867204	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (number of teeth)	0	0	1	1
rs9990343	4E-7	6.39794000867204	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	0	1	1	1
rs2484873	4E-7	6.39794000867204	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs2828520	4E-7	6.39794000867204	20125088	Genome-wide association study of recurrent early-onset major depressive disorder.	Major depressive disorder	1	1	1	1
rs457717	4E-7	6.39794000867204	20068591	A genome-wide association study for age-related hearing impairment in the Saami.	Hearing impairment	1	1	1	1
rs305061	4E-7	6.39794000867204	20062064	Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk.	Chronic lymphocytic leukemia	0	0	1	1
rs11668878	4E-7	6.39794000867204	20062064	Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk.	Chronic lymphocytic leukemia	0	0	1	1
rs1777672	4E-7	6.39794000867204	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	NA	NA	NA	NA
rs12274302	4E-7	6.39794000867204	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	NA	NA	NA	NA
rs6812193	4E-7	6.39794000867204	19915575	Genome-wide association study reveals genetic risk underlying Parkinson's disease.	Parkinson's disease	0	0	1	1
rs9630182	4E-7	6.39794000867204	19874204	IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study.	Bone mineral density	1	1	1	1
rs6110278	4E-7	6.39794000867204	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	1	1	1	1
rs10481151	4E-7	6.39794000867204	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs297325	4E-7	6.39794000867204	19714249	Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males.	Obesity and osteoporosis	1	1	1	1
rs2191566	4E-7	6.39794000867204	19684603	Germline genomic variants associated with childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs12554086	4E-7	6.39794000867204	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs1024020	4E-7	6.39794000867204	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs7023329	4E-7	6.39794000867204	19578364	Genome-wide association study identifies three loci associated with melanoma risk.	Melanoma	0	0	1	1
rs489693	4E-7	6.39794000867204	19557197	NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium.	Waist circumference	0	1	1	1
rs17153527	4E-7	6.39794000867204	19448619	Loci at chromosomes 13, 19 and 20 influence age at natural menopause.	Menopause (age at onset)	1	1	1	1
rs2269241	4E-7	6.39794000867204	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs1532085	4E-7	6.39794000867204	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	0	0	0
rs157580	4E-7	6.39794000867204	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	HDL cholesterol	0	1	0	0
rs2624265	4E-7	6.39794000867204	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	Metabolic traits	1	1	1	1
rs12753193	4E-7	6.39794000867204	19060910	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.	Metabolic traits	0	1	1	1
rs4453795	4E-7	6.39794000867204	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	1	1	1	1
rs12899449	4E-7	6.39794000867204	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	1	1	1	1
rs563694	4E-7	6.39794000867204	18521185	Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels.	Fasting plasma glucose	0	0	1	1
rs9303029	4E-7	6.39794000867204	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	0	0	0
rs8109578	4E-7	6.39794000867204	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs10871290	4E-7	6.39794000867204	18463975	A pilot genome-wide association study of early-onset breast cancer.	Breast cancer	0	1	1	1
rs9650315	4E-7	6.39794000867204	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	0	0	1	1
rs2040494	4E-7	6.39794000867204	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	0	0	1	1
rs5215	4E-7	6.39794000867204	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs17690232	4E-7	6.39794000867204	18193045	Common variants in the GDF5-UQCC region are associated with variation in human height.	Height	0	1	1	1
rs1376877	4E-7	6.39794000867204	17903303	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	Subclinical atherosclerosis traits (other)	0	1	1	1
rs1992660	4E-7	6.39794000867204	17684544	Systematic association mapping identifies NELL1 as a novel IBD disease gene.	Crohn's disease	0	0	1	1
rs11761231	4E-7	6.39794000867204	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Rheumatoid arthritis	1	1	1	1
rs4129148	4E-7	6.39794000867204	17522711	Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia.	Schizophrenia	NA	NA	NA	NA
rs10769945	5E-7	6.30102999566398	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	0	0	0	0
rs17206779	5E-7	6.30102999566398	23727862	Genome-wide association study identifies two susceptibility loci for osteosarcoma.	Osteosarcoma	1	1	1	1
rs4840097	5E-7	6.30102999566398	23577725	Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.	Age-related macular degeneration (smoking status interaction)	1	1	1	1
rs728996	5E-7	6.30102999566398	23633212	Genome-wide association of single-nucleotide polymorphisms with weight loss outcomes after Roux-en-Y gastric bypass surgery.	Weight loss (gastric bypass surgery)	1	1	1	1
rs9328321	5E-7	6.30102999566398	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	1	1	1	1
rs6097169	5E-7	6.30102999566398	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (non-asthmatics)	1	1	1	1
rs1408799	5E-7	6.30102999566398	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Eye color	0	1	1	1
rs78647349	5E-7	6.30102999566398	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs11770757	5E-7	6.30102999566398	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs7009219	5E-7	6.30102999566398	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs75617873	5E-7	6.30102999566398	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs4699587	5E-7	6.30102999566398	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs1994816	5E-7	6.30102999566398	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs2244613	5E-7	6.30102999566398	23467860	Genetic determinants of dabigatran plasma levels and their relation to bleeding.	Response to dabigatran etexilate treatment	NA	NA	NA	NA
rs2228468	5E-7	6.30102999566398	23314186	Genetic variation associated with circulating monocyte count in the eMERGE Network.	Monocyte count	1	1	1	1
rs2273788	5E-7	6.30102999566398	23314186	Genetic variation associated with circulating monocyte count in the eMERGE Network.	Monocyte count	1	1	1	1
rs2252865	5E-7	6.30102999566398	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs7045138	5E-7	6.30102999566398	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	NA	NA	NA	NA
rs3132935	5E-7	6.30102999566398	23894747	A comprehensive family-based replication study of schizophrenia genes.	Schizophrenia	0	0	0	0
rs6466479	5E-7	6.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs12342831	5E-7	6.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10822136	5E-7	6.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs8067912	5E-7	6.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9326244	5E-7	6.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6687262	5E-7	6.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7781977	5E-7	6.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6421315	5E-7	6.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10115586	5E-7	6.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9468811	5E-7	6.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11221522	5E-7	6.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA)	1	1	1	1
rs2830487	5E-7	6.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA-5-HIAA Factor score)	0	1	0	0
rs7483296	5E-7	6.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs17050244	5E-7	6.30102999566398	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	1	1	1	1
rs4779584	5E-7	6.30102999566398	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	0	0	1	1
rs9793739	5E-7	6.30102999566398	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs2206030   	5E-7	6.30102999566398	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs10513821   	5E-7	6.30102999566398	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs10777288   	5E-7	6.30102999566398	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs13290997   	5E-7	6.30102999566398	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs9308447	5E-7	6.30102999566398	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs16862782	5E-7	6.30102999566398	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs1029295	5E-7	6.30102999566398	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs13361160	5E-7	6.30102999566398	22956598	Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region.	Pain	1	1	1	1
rs8056742	5E-7	6.30102999566398	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	1	1	1	1
rs12651329	5E-7	6.30102999566398	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis (age of onset)	1	1	1	1
rs297941	5E-7	6.30102999566398	22889921	Genome-wide association study of obsessive-compulsive disorder.	Obsessive-compulsive disorder	1	1	1	1
rs4132699	5E-7	6.30102999566398	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs9380516	5E-7	6.30102999566398	22841784	Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.	Hepatitis C induced liver fibrosis	1	1	1	1
rs17372114	5E-7	6.30102999566398	22843503	Genome-wide association analysis identifies TYW3/CRYZ and NDST4 loci associated with circulating resistin levels.	Resistin levels 	1	1	1	1
rs6684428	5E-7	6.30102999566398	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs3810046	5E-7	6.30102999566398	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	1	1	1	1
rs13430864	5E-7	6.30102999566398	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	NA	NA	NA	NA
rs10760187	5E-7	6.30102999566398	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	1	1	1	1
rs2524005	5E-7	6.30102999566398	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs1198588	5E-7	6.30102999566398	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	0	0	1	1
rs12071951	5E-7	6.30102999566398	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	1	1	1	1
rs6598163	5E-7	6.30102999566398	22683712	Genome-wide association analysis identifies susceptibility loci for migraine without aura.	Migraine	1	1	1	1
rs727479	5E-7	6.30102999566398	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Estradiol levels	0	1	1	1
rs597800	5E-7	6.30102999566398	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Estradiol levels	0	1	1	1
rs13279522	5E-7	6.30102999566398	22666496	Genome-wide study of gene variants associated with differential cardiovascular event reduction by pravastatin therapy.	Response to statin therapy	1	1	1	1
rs3095748	5E-7	6.30102999566398	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs2043599	5E-7	6.30102999566398	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IFN-alpha)	1	1	1	1
rs3796352	5E-7	6.30102999566398	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted IL-2)	0	0	0	0
rs13006863	5E-7	6.30102999566398	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune reponse to smallpox (secreted TNF-alpha)	1	1	1	1
rs2973662	5E-7	6.30102999566398	22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Immune response to smallpox vaccine (IL-6)	NA	NA	NA	NA
rs2300835	5E-7	6.30102999566398	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	1	1	1	1
rs13166814	5E-7	6.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs1641895	5E-7	6.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs10495537	5E-7	6.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs7164176	5E-7	6.30102999566398	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs72991	5E-7	6.30102999566398	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs3129720	5E-7	6.30102999566398	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	0	1	1	1
rs2791553	5E-7	6.30102999566398	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	0	0	0
rs11190141	5E-7	6.30102999566398	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	0	0	1	1
rs1536076	5E-7	6.30102999566398	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	1	1	1	1
rs5994434	5E-7	6.30102999566398	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	1	1	1	1
rs6924995	5E-7	6.30102999566398	22331829	Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial.	Response to statin therapy (LDL-C)	0	1	1	1
rs786870	5E-7	6.30102999566398	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs391317	5E-7	6.30102999566398	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs6116492	5E-7	6.30102999566398	22137330	Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.	Creutzfeldt-Jakob disease (variant)	1	1	1	1
rs2742417	5E-7	6.30102999566398	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	1	1	1	1
rs8039808	5E-7	6.30102999566398	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	1	1	1	1
rs1466662	5E-7	6.30102999566398	22005931	Genome-wide association analysis of age-at-onset in Alzheimer's disease.	Alzheimer's disease (age of onset)	0	1	1	1
rs550448	5E-7	6.30102999566398	21980299	A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.	Type 1 diabetes	0	1	1	1
rs12914385	5E-7	6.30102999566398	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	1	1	1
rs13107325	5E-7	6.30102999566398	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Hypertension	0	1	0	0
rs7922491	5E-7	6.30102999566398	21907864	Identification of IL6R and chromosome 11q13.5 as risk loci for asthma.	Asthma	1	1	1	1
rs806321	5E-7	6.30102999566398	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs4075958	5E-7	6.30102999566398	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs307896	5E-7	6.30102999566398	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs2069762	5E-7	6.30102999566398	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	1	1	1
rs3117181	5E-7	6.30102999566398	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	0	0	1	1
rs12587311	5E-7	6.30102999566398	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs1406961	5E-7	6.30102999566398	21779381	Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study.	Cardiovascular disease risk factors	1	1	1	1
rs445114	5E-7	6.30102999566398	21743057	Genome-wide association study identifies new prostate cancer susceptibility loci.	Prostate cancer	0	0	1	1
rs55645543	5E-7	6.30102999566398	21685187	Genome-wide association study of smoking behaviours in patients with COPD.	Chronic obstructive pulmonary disease	NA	NA	NA	NA
rs1823172	5E-7	6.30102999566398	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs6964415	5E-7	6.30102999566398	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs10183640	5E-7	6.30102999566398	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs17665859	5E-7	6.30102999566398	21646302	Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels.	Bilirubin levels	1	1	1	1
rs1878022	5E-7	6.30102999566398	21483023	Genome-wide association study of survival in non-small cell lung cancer patients receiving platinum-based chemotherapy.	Response to platinum-based chemotherapy in non-small-cell lung cancer	1	1	1	1
rs987710	5E-7	6.30102999566398	21483845	Genome-wide association study identifies genetic loci associated with iron deficiency.	Iron status biomarkers	1	1	1	1
rs11636768	5E-7	6.30102999566398	21448238	Meta-analysis of genome-wide association for migraine in six population-based European cohorts.	Migraine	NA	NA	NA	NA
rs12938916	5E-7	6.30102999566398	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs1916521	5E-7	6.30102999566398	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	1	1	1	1
rs1245541	5E-7	6.30102999566398	21216879	A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3.	Insulin-like growth factors	1	1	1	1
rs2153960	5E-7	6.30102999566398	21216879	A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3.	Insulin-like growth factors	1	1	1	1
rs6503525	5E-7	6.30102999566398	21150878	Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia.	Asthma	0	0	1	1
rs2833556	5E-7	6.30102999566398	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Reasoning	1	1	1	1
rs7520258	5E-7	6.30102999566398	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Working memory	1	1	1	1
rs11214606	5E-7	6.30102999566398	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Working memory	1	1	1	1
rs12726652	5E-7	6.30102999566398	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Working memory	1	1	1	1
rs6800541	5E-7	6.30102999566398	21041692	Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science.	Atrioventricular conduction	0	1	1	1
rs401681	5E-7	6.30102999566398	20972438	A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.	Bladder cancer	0	1	1	1
rs239713	5E-7	6.30102999566398	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	AB1-42	1	1	1	1
rs12643654	5E-7	6.30102999566398	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	P-tau181p	1	1	1	1
rs2044117	5E-7	6.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs3890182	5E-7	6.30102999566398	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs1154155	5E-7	6.30102999566398	20711174	Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy.	Narcolepsy	0	0	1	1
rs641525	5E-7	6.30102999566398	20709820	Genome-wide association study identifies BICD1 as a susceptibility gene for emphysema.	Emphysema-related traits	1	1	1	1
rs2592394	5E-7	6.30102999566398	20700443	Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.	Magnesium levels	0	1	1	1
rs7178909	5E-7	6.30102999566398	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs12151790	5E-7	6.30102999566398	20548944	An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.	Osteoporosis	1	1	1	1
rs2380205	5E-7	6.30102999566398	20453838	Genome-wide association study identifies five new breast cancer susceptibility loci.	Breast cancer	1	1	1	1
rs1504749	5E-7	6.30102999566398	20364137	Genome-wide association study of intracranial aneurysm identifies three new risk loci.	Intracranial aneurysm	0	0	1	1
rs10906982	5E-7	6.30102999566398	20397748	Genome-wide association study of height and body mass index in Australian twin families.	Height	0	0	0	0
rs10994338	5E-7	6.30102999566398	20351715	Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.	Bipolar disorder and major depressive disorder (combined)	0	1	1	1
rs7584099	5E-7	6.30102999566398	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	0	1	1	1
rs10936599	5E-7	6.30102999566398	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs13118928	5E-7	6.30102999566398	20173748	Variants in FAM13A are associated with chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease	0	0	1	1
rs713155	5E-7	6.30102999566398	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs7140150	5E-7	6.30102999566398	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs8020441	5E-7	6.30102999566398	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	0	0	0	0
rs12063142	5E-7	6.30102999566398	20070850	Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.	Parkinson's disease	1	1	1	1
rs7169431	5E-7	6.30102999566398	20062064	Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk.	Chronic lymphocytic leukemia	1	1	1	1
rs2310173	5E-7	6.30102999566398	20062062	Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.	Ankylosing spondylitis	0	1	1	1
rs13394720	5E-7	6.30102999566398	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs16909898	5E-7	6.30102999566398	20010835	Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.	Pulmonary function	0	1	1	1
rs855791	5E-7	6.30102999566398	19820699	Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.	Iron status biomarkers	0	0	0	0
rs1800562	5E-7	6.30102999566398	19820699	Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.	Iron status biomarkers	0	0	0	0
rs10506328	5E-7	6.30102999566398	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Mean platelet volume	0	0	1	1
rs10767971	5E-7	6.30102999566398	19772629	Genomewide association study for onset age in Parkinson disease.	Parkinson's disease (age of onset)	1	1	1	1
rs6545977	5E-7	6.30102999566398	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	0	0	1	1
rs17727261	5E-7	6.30102999566398	19721433	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics.	Response to antipsychotic treatment	1	1	1	1
rs4756846	5E-7	6.30102999566398	19714249	Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males.	Obesity and osteoporosis	1	1	1	1
rs8015016	5E-7	6.30102999566398	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	QT interval	1	1	1	1
rs6068020	5E-7	6.30102999566398	19478329	Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia.	Male infertility	1	1	1	1
rs10841496	5E-7	6.30102999566398	19478329	Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia.	Male infertility	1	1	1	1
rs494620	5E-7	6.30102999566398	19448619	Loci at chromosomes 13, 19 and 20 influence age at natural menopause.	Menopause (age at onset)	0	0	1	1
rs16956936	5E-7	6.30102999566398	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs12714207	5E-7	6.30102999566398	19414484	Genome-wide association meta-analysis for total serum bilirubin levels.	Bilirubin levels	1	1	1	1
rs16886165	5E-7	6.30102999566398	19330030	A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).	Breast cancer	0	0	1	1
rs1980493	5E-7	6.30102999566398	19287509	Genome-wide association study of determinants of anti-cyclic citrullinated peptide antibody titer in adults with rheumatoid arthritis.	Anti-cyclic Citrullinated Peptide Antibody	0	1	1	1
rs2259816	5E-7	6.30102999566398	19198612	New susceptibility locus for coronary artery disease on chromosome 3q22.3.	Coronary heart disease	0	1	1	1
rs2870946	5E-7	6.30102999566398	19122664	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.	Ulcerative colitis	1	1	1	1
rs8321	5E-7	6.30102999566398	19115949	Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02).	AIDS progression	0	1	1	1
rs9623117	5E-7	6.30102999566398	19117981	Sequence variants at 22q13 are associated with prostate cancer risk.	Prostate cancer	0	0	1	1
rs17270561	5E-7	6.30102999566398	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	0	0	0
rs1517484	5E-7	6.30102999566398	18937294	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.	Attention deficit hyperactivity disorder (time to onset)	0	1	1	1
rs5219	5E-7	6.30102999566398	19056611	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data.	Type 2 diabetes	0	0	0	0
rs1382269	5E-7	6.30102999566398	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	1	1	1	1
rs9924951	5E-7	6.30102999566398	19043545	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Metabolite levels	1	1	1	1
rs2281597	5E-7	6.30102999566398	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs7046653	5E-7	6.30102999566398	18615156	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.	Response to TNF antagonist treatment	0	1	1	1
rs6918152	5E-7	6.30102999566398	18483556	A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.	Black vs. red hair color	0	1	0	0
rs11695685	5E-7	6.30102999566398	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs16957063	5E-7	6.30102999566398	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs4889294	5E-7	6.30102999566398	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs4779584	5E-7	6.30102999566398	18372905	A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.	Colorectal cancer	0	0	1	1
rs780094	5E-7	6.30102999566398	18179892	Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.	LDL cholesterol	0	1	1	1
rs7552393	5E-7	6.30102999566398	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	1	1	1	1
rs991258	5E-7	6.30102999566398	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	0	1	1	1
rs4831837	5E-7	6.30102999566398	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Morbidity-free survival	1	1	1	1
rs6556756	5E-7	6.30102999566398	17903305	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	Breast cancer	1	1	1	1
rs12708716	5E-7	6.30102999566398	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 1 diabetes	0	0	1	1
rs2836754	5E-7	6.30102999566398	17554261	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.	Crohn's disease	1	1	1	1
rs328	5E-7	6.30102999566398	17463246	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	Triglycerides	0	0	1	1
rs11065706	6E-7	6.22184874961636	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs17817449	6E-7	6.22184874961636	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	0	0	1	1
rs4752066	6E-7	6.22184874961636	23541324	Genome-wide association study identifies TH1 pathway genes associated with lung function in asthmatic patients.	Pulmonary function in asthmatics	1	1	1	1
rs117780815	6E-7	6.22184874961636	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs118048115	6E-7	6.22184874961636	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs7072122	6E-7	6.22184874961636	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs4761470	6E-7	6.22184874961636	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs10515260	6E-7	6.22184874961636	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs2235544	6E-7	6.22184874961636	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (hyperdiploidy)	0	1	1	1
rs723794	6E-7	6.22184874961636	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Smooth-surface caries 	1	1	1	1
rs11249608	6E-7	6.22184874961636	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	1	1	1	1
rs2721800	6E-7	6.22184874961636	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs9951150	6E-7	6.22184874961636	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	0	0	0
rs1480380	6E-7	6.22184874961636	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs1422438	6E-7	6.22184874961636	23419831	APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.	Alzheimer's disease biomarkers	1	1	1	1
rs334699	6E-7	6.22184874961636	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs17776563	6E-7	6.22184874961636	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs9468811	6E-7	6.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1054052	6E-7	6.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs13272236	6E-7	6.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4862046	6E-7	6.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4878639	6E-7	6.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs3097645	6E-7	6.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11128271	6E-7	6.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2745851	6E-7	6.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1747683	6E-7	6.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs13144232	6E-7	6.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs583583	6E-7	6.22184874961636	23382809	BCL9 and C9orf5 are associated with negative symptoms in schizophrenia: meta-analysis of two genome-wide association studies.	Schizophrenia (negative symptoms)	1	1	1	1
rs707824	6E-7	6.22184874961636	23349640	Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.	Lymphoma	1	1	1	1
rs948562	6E-7	6.22184874961636	23349640	Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.	Lymphoma	0	0	0	0
rs17810546	6E-7	6.22184874961636	23291587	Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.	Behcet's disease	0	1	1	1
rs12456874	6E-7	6.22184874961636	23180869	Genome-wide association study of survival in patients with pancreatic adenocarcinoma.	Pancreatic cancer	1	1	1	1
rs10242311	6E-7	6.22184874961636	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs189798	6E-7	6.22184874961636	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs16851055	6E-7	6.22184874961636	23041239	Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.	Stroke (ischemic)	1	1	1	1
rs12914385	6E-7	6.22184874961636	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	0	1	1	1
rs2303565	6E-7	6.22184874961636	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	0	1	1	1
rs771390	6E-7	6.22184874961636	22949513	Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32	Epilepsy (generalized)	1	1	1	1
rs10849605	6E-7	6.22184874961636	22899653	Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.	Lung cancer	1	1	1	1
rs4767234	6E-7	6.22184874961636	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	0	1	1	1
rs17057678	6E-7	6.22184874961636	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	1	1	1	1
rs9918668	6E-7	6.22184874961636	22773346	Linkage and association of successful aging to the 6q25 region in large Amish kindreds.	Aging	1	1	1	1
rs10948172	6E-7	6.22184874961636	22763110	Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study.	Osteoarthritis	0	1	1	1
rs7872515	6E-7	6.22184874961636	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1470579	6E-7	6.22184874961636	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs7833268	6E-7	6.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs1722636	6E-7	6.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs12204127	6E-7	6.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs743793	6E-7	6.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs6775909	6E-7	6.22184874961636	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	0	0	0	0
rs41418949	6E-7	6.22184874961636	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (time)	1	1	1	1
rs10520789	6E-7	6.22184874961636	22569225	Investigation of single nucleotide polymorphisms and biological pathways associated with response to TNFα inhibitors in patients with rheumatoid arthritis.	Response to TNF-alpha inhibitors in rheumatoid arthritis	1	1	1	1
rs6500395	6E-7	6.22184874961636	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs6026990	6E-7	6.22184874961636	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs4301033	6E-7	6.22184874961636	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	1	1	1	1
rs7834588	6E-7	6.22184874961636	22437554	Genome-wide association study identifies three common variants associated with serologic response to vitamin E supplementation in men.	Response to Vitamin E supplementation	1	1	1	1
rs7144584	6E-7	6.22184874961636	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs7792596	6E-7	6.22184874961636	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	1	1	1	1
rs12200560	6E-7	6.22184874961636	22319020	A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.	Coronary heart disease	0	1	1	1
rs1208285	6E-7	6.22184874961636	22306654	Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis.	Infantile hypertrophic pyloric stenosis	0	1	1	1
rs7191700	6E-7	6.22184874961636	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	0	1	1	1
rs1541374	6E-7	6.22184874961636	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	1	1	1
rs4409785	6E-7	6.22184874961636	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs756699	6E-7	6.22184874961636	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs2585617	6E-7	6.22184874961636	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs4963452	6E-7	6.22184874961636	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs6844153	6E-7	6.22184874961636	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs4789939	6E-7	6.22184874961636	21732829	Wnt signaling and Dupuytren's disease.	Dupuytren's disease	1	1	1	1
rs2823357	6E-7	6.22184874961636	21738487	Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.	Parkinson's disease	1	1	1	1
rs9296092	6E-7	6.22184874961636	21685187	Genome-wide association study of smoking behaviours in patients with COPD.	Chronic obstructive pulmonary disease	0	0	0	0
rs6716724	6E-7	6.22184874961636	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs6467710	6E-7	6.22184874961636	21502085	Genome-wide association study implicates PARD3B-based AIDS restriction.	AIDS progression	1	1	1	1
rs402219	6E-7	6.22184874961636	21493818	Genetic and clinical correlates of early-outgrowth colony-forming units.	Monocyte early outgrowth colony forming units	0	1	1	1
rs6495122	6E-7	6.22184874961636	21490707	Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.	Caffeine consumption	0	0	0	0
rs12148488	6E-7	6.22184874961636	21490707	Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.	Caffeine consumption	0	0	0	0
rs3752246	6E-7	6.22184874961636	21460841	Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.	Alzheimer's disease (late onset)	0	1	1	1
rs4787008	6E-7	6.22184874961636	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs525410	6E-7	6.22184874961636	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	0	1	1	1
rs10743430	6E-7	6.22184874961636	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Entorhinal cortical thickness	1	1	1	1
rs4611189	6E-7	6.22184874961636	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Reasoning	1	1	1	1
rs4805924	6E-7	6.22184874961636	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Working memory	1	1	1	1
rs4656940	6E-7	6.22184874961636	21102463	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.	Crohn's disease	0	0	1	1
rs1019238	6E-7	6.22184874961636	21668797	A genome-wide association study of DSM-IV cannabis dependence.	Cannabis dependence	1	1	1	1
rs17645023	6E-7	6.22184874961636	21057379	Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes.	Bipolar disorder and schizophrenia	1	1	1	1
rs2935776	6E-7	6.22184874961636	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	T-tau	1	1	1	1
rs4925189	6E-7	6.22184874961636	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	T-tau	1	1	1	1
rs6444931	6E-7	6.22184874961636	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1800562	6E-7	6.22184874961636	20927387	A genome-wide association study of red blood cell traits using the electronic medical record.	Red blood cell traits	0	0	0	0
rs794185	6E-7	6.22184874961636	20802204	Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis.	Multiple sclerosis--Brain Glutamate Levels	1	1	1	1
rs12912233	6E-7	6.22184874961636	20800221	Genome-wide association scan of trait depression.	Depression (quantitative trait)	1	1	1	1
rs10844154	6E-7	6.22184874961636	20709820	Genome-wide association study identifies BICD1 as a susceptibility gene for emphysema.	Emphysema-related traits	1	1	1	1
rs2710833	6E-7	6.22184874961636	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (AST)	1	1	1	1
rs6903896	6E-7	6.22184874961636	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs1562430	6E-7	6.22184874961636	20453838	Genome-wide association study identifies five new breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs4973768	6E-7	6.22184874961636	20453838	Genome-wide association study identifies five new breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs548097	6E-7	6.22184874961636	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	1	1	1	1
rs6504340	6E-7	6.22184874961636	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (number of teeth)	0	1	1	1
rs9386463	6E-7	6.22184874961636	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (time to first tooth eruption)	0	0	1	1
rs2429582	6E-7	6.22184874961636	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs11970254	6E-7	6.22184874961636	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs7873102	6E-7	6.22184874961636	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs12479254	6E-7	6.22184874961636	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs11643520	6E-7	6.22184874961636	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs7658637	6E-7	6.22184874961636	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs3934834	6E-7	6.22184874961636	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Body mass index	1	1	1	1
rs4118325	6E-7	6.22184874961636	19754311	Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03).	AIDS	0	1	1	1
rs5937496	6E-7	6.22184874961636	19734901	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	NA	NA	NA	NA
rs2229741	6E-7	6.22184874961636	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs17375901	6E-7	6.22184874961636	19597492	Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.	Atrial fibrillation	0	1	1	1
rs7544736	6E-7	6.22184874961636	19571811	Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.	Schizophrenia	0	0	1	1
rs4767631	6E-7	6.22184874961636	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	1	1	1	1
rs7175404	6E-7	6.22184874961636	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs1490388	6E-7	6.22184874961636	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs2054989	6E-7	6.22184874961636	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	0	1	1	1
rs6600671	6E-7	6.22184874961636	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	0	1	1	1
rs10515148	6E-7	6.22184874961636	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	1	1	1	1
rs7137869	6E-7	6.22184874961636	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Aging traits	1	1	1	1
rs11763353	7E-7	6.15490195998574	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Zn levels)	1	1	1	1
rs11232535	7E-7	6.15490195998574	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Zn levels)	1	1	1	1
rs406936	7E-7	6.15490195998574	23577725	Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.	Age-related macular degeneration	0	0	0	0
rs838147	7E-7	6.15490195998574	23636237	Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake.	Dietary macronutrient intake	0	0	0	0
rs13219957	7E-7	6.15490195998574	23620144	Genome-wide scan of job-related exhaustion with three replication studies implicate a susceptibility variant at the UST gene locus.	Job-related exhaustion	1	1	1	1
rs74566133	7E-7	6.15490195998574	23568457	Genetic variants associated with disordered eating.	Eating disorders (purging via substances) 	1	1	1	1
rs12475512	7E-7	6.15490195998574	23568457	Genetic variants associated with disordered eating.	Eating disorders (purging via substances) 	NA	NA	NA	NA
rs4836694	7E-7	6.15490195998574	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs326946	7E-7	6.15490195998574	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs2046315	7E-7	6.15490195998574	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Pit-and-Fissure caries 	0	1	0	0
rs6659742	7E-7	6.15490195998574	23472185	Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.	Multiple sclerosis (OCB status)	1	1	1	1
rs17692896	7E-7	6.15490195998574	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs17779457	7E-7	6.15490195998574	23376709	A 2-stage genome-wide association study to identify single nucleotide polymorphisms associated with development of urinary symptoms after radiotherapy for prostate cancer.	Urinary symptoms in response to radiotherapy in prostate cancer	0	1	1	1
rs10822136	7E-7	6.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6132333	7E-7	6.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs16863118	7E-7	6.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1095368	7E-7	6.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4720952	7E-7	6.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs9403856	7E-7	6.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs7902091	7E-7	6.15490195998574	23358160	Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.	Schizophrenia (cytomegalovirus infection interaction)	1	1	1	1
rs12906542	7E-7	6.15490195998574	23354978	Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation.	Breast cancer	1	1	1	1
rs55681231	7E-7	6.15490195998574	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs7209395	7E-7	6.15490195998574	23279374	Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain.	β2-Glycoprotein I (β2-GPI) plasma levels	0	1	1	1
rs17074636	7E-7	6.15490195998574	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Gout	1	1	1	1
rs1933737	7E-7	6.15490195998574	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs11099098	7E-7	6.15490195998574	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs8040868   	7E-7	6.15490195998574	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs3734729   	7E-7	6.15490195998574	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs2333194	7E-7	6.15490195998574	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	1	1	1	1
rs12602978	7E-7	6.15490195998574	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs11223996	7E-7	6.15490195998574	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs11723864	7E-7	6.15490195998574	23028342	New susceptibility loci associated with kidney disease in type 1 diabetes.	Type 1 diabetes nephropathy	1	1	1	1
rs11082762	7E-7	6.15490195998574	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	0	1	1	1
rs4534959	7E-7	6.15490195998574	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs6040399	7E-7	6.15490195998574	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	1	1	1	1
rs2050190	7E-7	6.15490195998574	22703881	Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.	Activated partial thromboplastin time	0	1	1	1
rs9810233	7E-7	6.15490195998574	22704111	Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.	Erectile dysfunction	1	1	1	1
rs11220082	7E-7	6.15490195998574	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	0	1	1	1
rs16915157	7E-7	6.15490195998574	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	0	1	1	1
rs10514317	7E-7	6.15490195998574	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Sex hormone-binding globulin levels	1	1	1	1
rs7996217	7E-7	6.15490195998574	22628157	Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults.	HIV-associated dementia 	NA	NA	NA	NA
rs7034200	7E-7	6.15490195998574	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs13273088	7E-7	6.15490195998574	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	1	1	1	1
rs12591650	7E-7	6.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs17501712	7E-7	6.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs16909318	7E-7	6.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs9821642	7E-7	6.15490195998574	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	0	0	0	0
rs9604529	7E-7	6.15490195998574	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs1914816	7E-7	6.15490195998574	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs17697518	7E-7	6.15490195998574	22484627	A genome-wide association meta-analysis identifies new childhood obesity loci.	Obesity	1	1	1	1
rs1889321	7E-7	6.15490195998574	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs10510829	7E-7	6.15490195998574	22379998	Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.	Adverse response to lamotrigine and phenytoin	1	1	1	1
rs12719740	7E-7	6.15490195998574	22354554	Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13.	Arthritis (juvenile idiopathic)	1	1	1	1
rs1875620	7E-7	6.15490195998574	22331829	Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial.	Response to statin therapy (LDL-C)	1	1	1	1
rs2229238	7E-7	6.15490195998574	22319020	A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.	Coronary heart disease	0	1	1	1
rs17564315	7E-7	6.15490195998574	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	0	0	0	0
rs1396485	7E-7	6.15490195998574	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs10888935	7E-7	6.15490195998574	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs6517147	7E-7	6.15490195998574	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs1799990	7E-7	6.15490195998574	22210626	Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.	Prion diseases	0	1	1	1
rs9596270	7E-7	6.15490195998574	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	1	1	1	1
rs10866713	7E-7	6.15490195998574	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	1	1	1	1
rs16861531	7E-7	6.15490195998574	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	1	1	1	1
rs17513503	7E-7	6.15490195998574	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	Allergic rhinitis	0	1	0	0
rs2036527	7E-7	6.15490195998574	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	0	0	0
rs9371601	7E-7	6.15490195998574	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	0	1	1	1
rs1878406	7E-7	6.15490195998574	21909108	Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.	Carotid intima media thickness	0	0	0	0
rs2521501	7E-7	6.15490195998574	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Hypertension	0	1	0	0
rs10936599	7E-7	6.15490195998574	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs415430	7E-7	6.15490195998574	21812969	Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.	Parkinson's disease	0	0	0	0
rs9581094	7E-7	6.15490195998574	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs10833905	7E-7	6.15490195998574	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs10953454	7E-7	6.15490195998574	21552555	A genome-wide association study on obesity and obesity-related traits.	Obesity	1	1	1	1
rs5762430	7E-7	6.15490195998574	21552555	A genome-wide association study on obesity and obesity-related traits.	Obesity	1	1	1	1
rs17081231	7E-7	6.15490195998574	21552555	A genome-wide association study on obesity and obesity-related traits.	Obesity	1	1	1	1
rs6716455	7E-7	6.15490195998574	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (alcohol use disorder factor score)	1	1	1	1
rs13064954	7E-7	6.15490195998574	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs514636	7E-7	6.15490195998574	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs3729931	7E-7	6.15490195998574	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	0	1	1	1
rs3747767	7E-7	6.15490195998574	21302353	Genome-wide association study of hoarding traits.	Hoarding	1	1	1	1
rs11849538	7E-7	6.15490195998574	21172079	Genome-wide case-control study of musculoskeletal adverse events and functional genomics in women receiving aromatase inhibitors: going beyond associations.	Adverse response to aromatase inhibitors	1	1	1	1
rs11677416	7E-7	6.15490195998574	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Working memory	1	1	1	1
rs1937332	7E-7	6.15490195998574	21041692	Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science.	Atrioventricular conduction	1	1	1	1
rs11209026	7E-7	6.15490195998574	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	0	1	1	1
rs610604	7E-7	6.15490195998574	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	0	0	1	1
rs10496702	7E-7	6.15490195998574	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs7716600	7E-7	6.15490195998574	20872241	A combined analysis of genome-wide association studies in breast cancer.	Breast cancer	0	0	1	1
rs12150338	7E-7	6.15490195998574	20705733	Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.	Calcium levels	0	1	1	1
rs2645424	7E-7	6.15490195998574	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs7866070	7E-7	6.15490195998574	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs525455	7E-7	6.15490195998574	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	1	1	1	1
rs2823819	7E-7	6.15490195998574	20732626	Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	1	1	1	1
rs11074889	7E-7	6.15490195998574	20732626	Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	1	1	1	1
rs13119723	7E-7	6.15490195998574	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs909116	7E-7	6.15490195998574	20453838	Genome-wide association study identifies five new breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs2210327	7E-7	6.15490195998574	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	1	1	1	1
rs3764261	7E-7	6.15490195998574	20385819	Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.	Age-related macular degeneration	0	0	1	1
rs16920624	7E-7	6.15490195998574	20360315	Genome-wide pharmacogenetics of antidepressant response in the GENDEP project.	Response to antidepressants	1	1	1	1
rs16883019	7E-7	6.15490195998574	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs9664222	7E-7	6.15490195998574	20304771	A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium.	Longevity	1	1	1	1
rs2762051	7E-7	6.15490195998574	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs10511089	7E-7	6.15490195998574	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs401681	7E-7	6.15490195998574	20101243	A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33.	Pancreatic cancer	0	1	1	1
rs1106634	7E-7	6.15490195998574	20038947	Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.	Major depressive disorder (broad)	1	1	1	1
rs12518099	7E-7	6.15490195998574	19734900	Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia.	Type 2 diabetes and other traits	1	1	1	1
rs3744064	7E-7	6.15490195998574	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs10781380	7E-7	6.15490195998574	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs6845865	7E-7	6.15490195998574	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	QT interval	1	1	1	1
rs789852	7E-7	6.15490195998574	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	QT interval	1	1	1	1
rs7910620	7E-7	6.15490195998574	19584346	Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.	Cardiac structure and function	1	1	1	1
rs1790100	7E-7	6.15490195998574	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	0	1	1	1
rs9814870	7E-7	6.15490195998574	19478329	Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia.	Male infertility	1	1	1	1
rs4955755	7E-7	6.15490195998574	19448619	Loci at chromosomes 13, 19 and 20 influence age at natural menopause.	Menopause (age at onset)	1	1	1	1
rs11014166	7E-7	6.15490195998574	19430479	Genome-wide association study of blood pressure and hypertension.	Systolic blood pressure	0	1	0	0
rs17122021	7E-7	6.15490195998574	19207018	Genome-wide association study of acute post-surgical pain in humans.	Pain	1	1	1	1
rs1007738	7E-7	6.15490195998574	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (hip)	0	0	1	1
rs12272004	7E-7	6.15490195998574	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	0	0	0
rs10811661	7E-7	6.15490195998574	19056611	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data.	Type 2 diabetes	0	0	1	1
rs10946398	7E-7	6.15490195998574	19056611	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data.	Type 2 diabetes	0	0	1	1
rs1564282	7E-7	6.15490195998574	18985386	Genomewide association study for susceptibility genes contributing to familial Parkinson disease.	Parkinson's disease (familial)	0	1	1	1
rs12883384	7E-7	6.15490195998574	18762592	Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism.	Neuroticism	1	1	1	1
rs4950322	7E-7	6.15490195998574	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	0	0	0
rs17415853	7E-7	6.15490195998574	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs12199222	7E-7	6.15490195998574	18391951	Many sequence variants affecting diversity of adult human height.	Height	1	1	1	1
rs7209435	7E-7	6.15490195998574	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs1452928	7E-7	6.15490195998574	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	1	1	1	1
rs10497721	7E-7	6.15490195998574	17903298	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	Diabetes (incident)	1	1	1	1
rs1154865	7E-7	6.15490195998574	17903305	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	Breast cancer	0	1	1	1
rs11052552	7E-7	6.15490195998574	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 1 diabetes	0	0	0	0
rs7506045	7E-7	6.15490195998574	17434096	A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.	Stroke	1	1	1	1
rs693	7E-7	6.15490195998574	17463246	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	Triglycerides	0	0	1	1
rs4363506	7E-7	6.15490195998574	17362836	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.	Amyotrophic lateral sclerosis	1	1	1	1
rs11897432	8E-7	6.09691001300806	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	0	1	1	1
rs724210	8E-7	6.09691001300806	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	1	1	1	1
rs4780805	8E-7	6.09691001300806	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep duration	1	1	1	1
rs7322916	8E-7	6.09691001300806	23568457	Genetic variants associated with disordered eating.	Eating disorders	1	1	1	1
rs62531686	8E-7	6.09691001300806	23555189	Genome-wide association study identifies genetic determinants of urine PCA3 levels in men.	PCA3 expression level	1	1	1	1
rs11196174	8E-7	6.09691001300806	23544013	Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.	Breast Cancer in BRCA1 mutation carriers	0	1	1	1
rs143954261	8E-7	6.09691001300806	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs73660619	8E-7	6.09691001300806	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs2302777	8E-7	6.09691001300806	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (hyperdiploidy)	0	1	1	1
rs2055729	8E-7	6.09691001300806	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (hyperdiploidy)	1	1	1	1
rs17411949	8E-7	6.09691001300806	23472185	Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.	Multiple sclerosis (OCB status)	1	1	1	1
rs3826782	8E-7	6.09691001300806	23459936	Exploring the genetic basis of chronic periodontitis: a genome-wide association study.	Periodontitis	1	1	1	1
rs4764124	8E-7	6.09691001300806	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	1	1	1	1
rs10780944	8E-7	6.09691001300806	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	1	1	1	1
rs113524839	8E-7	6.09691001300806	23419831	APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.	Alzheimer's disease biomarkers	1	1	1	1
rs11710456	8E-7	6.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2530544	8E-7	6.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2764743	8E-7	6.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10226930	8E-7	6.09691001300806	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs7483296	8E-7	6.09691001300806	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA/ MHPG Ratio)	0	1	0	0
rs187075894	8E-7	6.09691001300806	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs10042968	8E-7	6.09691001300806	23216389	Genome-wide significant association signals in IPO11-HTR1A region specific for alcohol and nicotine codependence.	Alcohol and nictotine co-dependence	0	0	0	0
rs10054504	8E-7	6.09691001300806	23184150	Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer.	Renal cell carcinoma	1	1	1	1
rs2280401	8E-7	6.09691001300806	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum albumin level	0	0	0	0
rs878889	8E-7	6.09691001300806	23028342	New susceptibility loci associated with kidney disease in type 1 diabetes.	Type 1 diabetes nephropathy	1	1	1	1
rs12361953	8E-7	6.09691001300806	22881374	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	Alzheimer's disease (late onset)	1	1	1	1
rs1873147	8E-7	6.09691001300806	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	0	1	1	1
rs4441471	8E-7	6.09691001300806	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs7711337	8E-7	6.09691001300806	22843504	Individual common variants exert weak effects on the risk for autism spectrum disorderspi.	Autism	1	1	1	1
rs7834018	8E-7	6.09691001300806	22843504	Individual common variants exert weak effects on the risk for autism spectrum disorderspi.	Autism	1	1	1	1
rs715921	8E-7	6.09691001300806	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs16889038	8E-7	6.09691001300806	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs9536318	8E-7	6.09691001300806	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs1417205	8E-7	6.09691001300806	22823124	The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation.	Cannabis use (initiation)	1	1	1	1
rs61280460	8E-7	6.09691001300806	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs12742923	8E-7	6.09691001300806	22628157	Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults.	HIV-associated dementia 	1	1	1	1
rs2838923	8E-7	6.09691001300806	22745009	Multiple loci influencing hippocampal degeneration identified by genome scan.	Hippocampal atrophy	1	1	1	1
rs3783938	8E-7	6.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs436000	8E-7	6.09691001300806	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (fairness)	0	0	0	0
rs1329568	8E-7	6.09691001300806	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs16906916	8E-7	6.09691001300806	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs6432018	8E-7	6.09691001300806	22174390	Heritability of submaximal exercise heart rate response to exercise training is accounted for by nine SNPs.	Heart rate variability traits	1	1	1	1
rs1993976	8E-7	6.09691001300806	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	1	1	1	1
rs17170316	8E-7	6.09691001300806	21993531	Genome-wide association study does not reveal major genetic determinants for anti-cytomegalovirus antibody response.	Cytomegalovirus antibody response	1	1	1	1
rs8111998	8E-7	6.09691001300806	21979947	A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.	Corneal structure	1	1	1	1
rs6547853	8E-7	6.09691001300806	21980299	A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.	Type 1 diabetes	0	1	1	1
rs10786436	8E-7	6.09691001300806	21980299	A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.	Type 1 diabetes	1	1	1	1
rs932764	8E-7	6.09691001300806	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Diastolic blood pressure	0	1	0	0
rs3774372	8E-7	6.09691001300806	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs16868941	8E-7	6.09691001300806	21876539	Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM.	Coffee consumption	1	1	1	1
rs12459897	8E-7	6.09691001300806	21829377	Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.	Phospholipid levels (plasma)	1	1	1	1
rs10488631	8E-7	6.09691001300806	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	0	0	0
rs4975709	8E-7	6.09691001300806	21779381	Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study.	Cardiovascular disease risk factors	1	1	1	1
rs1047964	8E-7	6.09691001300806	21779381	Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study.	Cardiovascular disease risk factors	1	1	1	1
rs4932194	8E-7	6.09691001300806	21732829	Wnt signaling and Dupuytren's disease.	Dupuytren's disease	1	1	1	1
rs2468677	8E-7	6.09691001300806	21700879	Novel locus FER is associated with serum HMW adiponectin levels.	Adiponectin levels	1	1	1	1
rs54211	8E-7	6.09691001300806	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	0	1	1	1
rs1949733	8E-7	6.09691001300806	21659360	Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial.	Response to antineoplastic agents	1	1	1	1
rs1342899	8E-7	6.09691001300806	21659360	Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial.	Response to antineoplastic agents	1	1	1	1
rs365302	8E-7	6.09691001300806	21606135	A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.	Coronary heart disease	1	1	1	1
rs9923451	8E-7	6.09691001300806	21552555	A genome-wide association study on obesity and obesity-related traits.	Obesity	1	1	1	1
rs9556711	8E-7	6.09691001300806	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (alcohol dependence factor score)	1	1	1	1
rs1054627	8E-7	6.09691001300806	21533022	Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.	Bone mineral density	0	1	1	1
rs7208487	8E-7	6.09691001300806	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	0	1	1	1
rs13080594	8E-7	6.09691001300806	21368711	Genome-wide association study of personality traits in bipolar patients.	Personality dimensions	1	1	1	1
rs17190927	8E-7	6.09691001300806	21368711	Genome-wide association study of personality traits in bipolar patients.	Personality dimensions	1	1	1	1
rs1772408	8E-7	6.09691001300806	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	1	1	1	1
rs152528	8E-7	6.09691001300806	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	1	1	1	1
rs10510181	8E-7	6.09691001300806	21216876	Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.	Scoliosis	0	1	1	1
rs10475598	8E-7	6.09691001300806	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs6856328	8E-7	6.09691001300806	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Working memory	1	1	1	1
rs3743266	8E-7	6.09691001300806	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	1	1	1	1
rs17075286	8E-7	6.09691001300806	21057379	Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes.	Bipolar disorder and schizophrenia	1	1	1	1
rs12745968	8E-7	6.09691001300806	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs11143230	8E-7	6.09691001300806	20877300	Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project.	Suicidal ideation	1	1	1	1
rs7158782	8E-7	6.09691001300806	20876420	Genome-wide associations and functional genomic studies of musculoskeletal adverse events in women receiving aromatase inhibitors.	Adverse response to aromatase inhibitors	0	0	1	1
rs7905537	8E-7	6.09691001300806	20709820	Genome-wide association study identifies BICD1 as a susceptibility gene for emphysema.	Emphysema-related traits	1	1	1	1
rs887304	8E-7	6.09691001300806	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (lobular)	1	1	1	1
rs2270447	8E-7	6.09691001300806	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs10431058	8E-7	6.09691001300806	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs425215	8E-7	6.09691001300806	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	NA	NA	NA	NA
rs13263959	8E-7	6.09691001300806	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Hair color	1	1	1	1
rs13031237	8E-7	6.09691001300806	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	0	1	1
rs9674544	8E-7	6.09691001300806	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (time to first tooth eruption)	0	0	0	0
rs9473582	8E-7	6.09691001300806	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	0	1	1	1
rs17718580	8E-7	6.09691001300806	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	0	0	0	0
rs11970286	8E-7	6.09691001300806	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	1	1	1
rs17144465	8E-7	6.09691001300806	20038947	Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.	Major depressive disorder (broad)	1	1	1	1
rs1471403	8E-7	6.09691001300806	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (hip)	0	1	0	0
rs10498514	8E-7	6.09691001300806	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs652889	8E-7	6.09691001300806	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	QT interval	1	1	1	1
rs4318720	8E-7	6.09691001300806	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	QT interval	1	1	1	1
rs10935268	8E-7	6.09691001300806	19578179	A genome-wide association study of acenocoumarol maintenance dosage.	Acenocoumarol maintenance dosage	1	1	1	1
rs7138803	8E-7	6.09691001300806	19557197	NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium.	Waist circumference	0	1	1	1
rs409045	8E-7	6.09691001300806	19454037	Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study.	Left ventricular mass	1	1	1	1
rs12206204	8E-7	6.09691001300806	19414484	Genome-wide association meta-analysis for total serum bilirubin levels.	Bilirubin levels	1	1	1	1
rs2274089	8E-7	6.09691001300806	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	0	0	0
rs522958	8E-7	6.09691001300806	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Hyperactive-impulsive symptoms	1	1	1	1
rs397020	8E-7	6.09691001300806	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs10514604	8E-7	6.09691001300806	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs6472866	8E-7	6.09691001300806	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs4742971	8E-7	6.09691001300806	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs11898505	8E-7	6.09691001300806	18445777	Multiple genetic loci for bone mineral density and fractures.	Bone mineral density (spine)	0	0	1	1
rs6733301	8E-7	6.09691001300806	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs314268	8E-7	6.09691001300806	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs2326458	8E-7	6.09691001300806	18391951	Many sequence variants affecting diversity of adult human height.	Height	1	1	1	1
rs6088792	8E-7	6.09691001300806	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs7466269	8E-7	6.09691001300806	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	0	0	1	1
rs4932217	8E-7	6.09691001300806	18193045	Common variants in the GDF5-UQCC region are associated with variation in human height.	Height	0	1	1	1
rs2144300	8E-7	6.09691001300806	18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	Triglycerides	0	0	0	0
rs746961	8E-7	6.09691001300806	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	1	1	1	1
rs2820037	8E-7	6.09691001300806	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Hypertension	1	1	1	1
rs2412488	9E-7	6.04575749056067	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	1	1	1	1
rs11084337	9E-7	6.04575749056067	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Se levels)	1	1	1	1
rs1799922	9E-7	6.04575749056067	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (time to first tooth eruption)	0	1	0	0
rs1390943	9E-7	6.04575749056067	23620142	Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.	Circulating myeloperoxidase levels (serum) 	0	1	1	1
rs236373	9E-7	6.04575749056067	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs142014203	9E-7	6.04575749056067	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs12520016	9E-7	6.04575749056067	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Eye color	1	1	1	1
rs2421847	9E-7	6.04575749056067	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs116348108	9E-7	6.04575749056067	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs17112190	9E-7	6.04575749056067	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs780179	9E-7	6.04575749056067	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs10975519	9E-7	6.04575749056067	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	1	1	1	1
rs4959027	9E-7	6.04575749056067	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs548181	9E-7	6.04575749056067	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs4271113	9E-7	6.04575749056067	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	NA	NA	NA	NA
rs7174755	9E-7	6.04575749056067	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	0	0	0	0
rs12828421	9E-7	6.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11710456	9E-7	6.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4466877	9E-7	6.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2060070	9E-7	6.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2745851	9E-7	6.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs12922317	9E-7	6.04575749056067	23358160	Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.	Schizophrenia	0	1	1	1
rs10809457 	9E-7	6.04575749056067	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitic acid (16:0) plasma levels	NA	NA	NA	NA
rs10414689 	9E-7	6.04575749056067	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitic acid (16:0) plasma levels	NA	NA	NA	NA
rs3135753	9E-7	6.04575749056067	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Gout	NA	NA	NA	NA
rs13181	9E-7	6.04575749056067	23108145	Genome-wide association study reveals novel genetic determinants of DNA repair capacity in lung cancer.	Lung Cancer (DNA repair capacity)	0	1	1	1
rs2531154	9E-7	6.04575749056067	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs7849581	9E-7	6.04575749056067	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs2483058	9E-7	6.04575749056067	23031429	A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol.	Cholesterol and Triglycerides	1	1	1	1
rs9301951	9E-7	6.04575749056067	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs2006933	9E-7	6.04575749056067	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	1	1	1	1
rs1997352	9E-7	6.04575749056067	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	0	1	1	1
rs6764050	9E-7	6.04575749056067	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	1	1	1	1
rs11621969	9E-7	6.04575749056067	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	1	1	1	1
rs17040430	9E-7	6.04575749056067	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder	1	1	1	1
rs886424	9E-7	6.04575749056067	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs10503256	9E-7	6.04575749056067	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Schizophrenia	0	0	1	1
rs909814	9E-7	6.04575749056067	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Testosterone levels	1	1	1	1
rs1316952	9E-7	6.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	0	0	0
rs2299587	9E-7	6.04575749056067	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs9820695	9E-7	6.04575749056067	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	0	0	0	0
rs6774280	9E-7	6.04575749056067	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs1273516	9E-7	6.04575749056067	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	0	1	1	1
rs13137105	9E-7	6.04575749056067	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs3113494	9E-7	6.04575749056067	22470424	A high-density genome-wide association screen of sporadic ALS in US veterans.	Amyotrophic lateral sclerosis	1	1	1	1
rs2275336	9E-7	6.04575749056067	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	1	1	1	1
rs11713158	9E-7	6.04575749056067	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	1	1	1	1
rs13122273	9E-7	6.04575749056067	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs3809346	9E-7	6.04575749056067	22144573	Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.	Coronary artery calcification	0	1	1	1
rs290986	9E-7	6.04575749056067	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs11158493	9E-7	6.04575749056067	21659360	Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial.	Response to antineoplastic agents	1	1	1	1
rs7524102	9E-7	6.04575749056067	21533022	Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.	Bone mineral density	0	1	1	1
rs9866141	9E-7	6.04575749056067	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	0	0	0	0
rs17388568	9E-7	6.04575749056067	21297633	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.	Ulcerative colitis	0	1	1	1
rs6844851	9E-7	6.04575749056067	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	0	0	1	1
rs708547	9E-7	6.04575749056067	21106707	A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity.	Bleomycin sensitivity	0	1	1	1
rs17126180	9E-7	6.04575749056067	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Reasoning	1	1	1	1
rs1431318	9E-7	6.04575749056067	21668797	A genome-wide association study of DSM-IV cannabis dependence.	Cannabis dependence	0	0	0	0
rs12534221	9E-7	6.04575749056067	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	AB1-42	1	1	1	1
rs5998432	9E-7	6.04575749056067	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	T-tau	1	1	1	1
rs6591182	9E-7	6.04575749056067	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (lobular)	0	1	1	1
rs2014357	9E-7	6.04575749056067	20585627	Web-based, participant-driven studies yield novel genetic associations for common traits.	Common traits (Other)	1	1	1	1
rs12808199	9E-7	6.04575749056067	20548944	An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.	Osteoporosis	1	1	1	1
rs17184557	9E-7	6.04575749056067	20548944	An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.	Osteoporosis	1	1	1	1
rs2872507	9E-7	6.04575749056067	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs4684585	9E-7	6.04575749056067	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs10506525	9E-7	6.04575749056067	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (number of teeth)	0	0	0	0
rs11696501	9E-7	6.04575749056067	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs4296809	9E-7	6.04575749056067	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	0	1	1	1
rs17691394	9E-7	6.04575749056067	20009918	A genome-wide association study of carotid atherosclerosis in HIV-infected men.	Carotid atherosclerosis in HIV infection	1	1	1	1
rs17132261	9E-7	6.04575749056067	19584346	Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.	Cardiac structure and function	1	1	1	1
rs7474896	9E-7	6.04575749056067	19553259	Common body mass index-associated variants confer risk of extreme obesity.	Obesity (extreme)	1	1	1	1
rs1399645	9E-7	6.04575749056067	19478329	Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia.	Male infertility	1	1	1	1
rs17007695	9E-7	6.04575749056067	19176441	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.	Response to treatment for acute lymphoblastic leukemia	1	1	1	1
rs1569175	9E-7	6.04575749056067	19176441	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.	Response to treatment for acute lymphoblastic leukemia	1	1	1	1
rs227584	9E-7	6.04575749056067	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (hip)	0	0	1	1
rs12670798	9E-7	6.04575749056067	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Cholesterol, total	0	0	0	0
rs644148	9E-7	6.04575749056067	18957941	Genome-wide association scan for five major dimensions of personality.	Personality dimensions	1	1	1	1
rs2212361	9E-7	6.04575749056067	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Attention deficit hyperactivity disorder symptoms (interaction)	1	1	1	1
rs2814828	9E-7	6.04575749056067	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs2554380	9E-7	6.04575749056067	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs7341475	9E-7	6.04575749056067	18282107	Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women.	Schizophrenia	0	1	1	1
rs2639889	9E-7	6.04575749056067	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Morbidity-free survival	1	1	1	1
rs3814219	9E-7	6.04575749056067	17903301	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	Endothelial function traits	0	1	1	1
rs9930506	9E-7	6.04575749056067	17658951	Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits.	Obesity-related traits	0	0	0	0
rs3763558	1E-6	6	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	1	1	1	1
rs2086452	1E-6	6	23727862	Genome-wide association study identifies two susceptibility loci for osteosarcoma.	Osteosarcoma	1	1	1	1
rs679711	1E-6	6	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep depth	1	1	1	1
rs1986116	1E-6	6	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep quality	1	1	1	1
rs10014072	1E-6	6	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Cu levels)	1	1	1	1
rs7226229	1E-6	6	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Se levels)	1	1	1	1
rs10789336	1E-6	6	23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Body mass index	0	0	1	1
rs12049351	1E-6	6	23620142	Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.	Circulating myeloperoxidase levels (plasma)	1	1	1	1
rs2441727	1E-6	6	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	1	1	1	1
rs56156506	1E-6	6	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	NA	NA	NA	NA
rs77600076	1E-6	6	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs13077017	1E-6	6	23568457	Genetic variants associated with disordered eating.	Eating disorders (purging via substances) 	0	1	1	1
rs2275848	1E-6	6	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	1	1	1	1
rs8074700	1E-6	6	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (non-asthmatics)	0	1	1	1
rs4336372	1E-6	6	23555300	Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis.	Response to anti-TNF treatment in rheumatoid arthritis	1	1	1	1
rs2392492	1E-6	6	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs17172199	1E-6	6	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs16832889	1E-6	6	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs17042688	1E-6	6	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	0	0	0	0
rs10501858	1E-6	6	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs12620464	1E-6	6	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs6077414	1E-6	6	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs478665	1E-6	6	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs727333	1E-6	6	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs10509328	1E-6	6	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs8192935	1E-6	6	23467860	Genetic determinants of dabigatran plasma levels and their relation to bleeding.	Response to dabigatran etexilate treatment	1	1	1	1
rs2270221	1E-6	6	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	1	1	1	1
rs12449465	1E-6	6	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	1	1	1	1
rs12325410	1E-6	6	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs6694545	1E-6	6	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs12443954	1E-6	6	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs12871532	1E-6	6	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs13418455	1E-6	6	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs4650608	1E-6	6	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs8060581	1E-6	6	23509613	Genome-wide association study of antiphospholipid antibodies.	Presence of antiphospholipid antibodies	1	1	1	1
rs7702276	1E-6	6	23419831	APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.	Alzheimer's disease biomarkers	1	1	1	1
rs13279485	1E-6	6	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs7924357	1E-6	6	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs2920001	1E-6	6	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs1960445	1E-6	6	23396134	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.	Refractive error	NA	NA	NA	NA
rs6499766	1E-6	6	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs657152	1E-6	6	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs1571583	1E-6	6	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs12140439	1E-6	6	23894747	A comprehensive family-based replication study of schizophrenia genes.	Schizophrenia	1	1	1	1
rs10484358	1E-6	6	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs6799788	1E-6	6	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	0	1	1	1
rs9948784	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs17403780	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs918629	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs17719439	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1794265	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs11774682	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10852453	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6132333	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs9263963	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs11820502	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs17161553	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10108033	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6102185	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs16952065	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs3780486	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11738945	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7700895	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs8067912	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2745851	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6794649	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs4711279	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs9886428	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1023721	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6479779	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs1650123	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4878639	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs756777	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11568995	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7582701	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11958404	1E-6	6	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1440620	1E-6	6	23372041	Novel locus including FGF21 is associated with dietary macronutrient intake.	Dietary macronutrient intake	1	1	1	1
rs10980508	1E-6	6	23386860	Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes.	Type 2 diabetes (dietary heme iron intake interaction)	1	1	1	1
rs8057927	1E-6	6	23358160	Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.	Schizophrenia	1	1	1	1
rs17648246 	1E-6	6	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Oleic acid (18:1n-9) plasma levels	NA	NA	NA	NA
rs3134950 	1E-6	6	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Oleic acid (18:1n-9) plasma levels	NA	NA	NA	NA
rs334809 	1E-6	6	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Oleic acid (18:1n-9) plasma levels	NA	NA	NA	NA
rs10237735 	1E-6	6	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitic acid (16:0) plasma levels	NA	NA	NA	NA
rs11120822 	1E-6	6	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Stearic acid (18:0) plasma levels	NA	NA	NA	NA
rs643410	1E-6	6	23382809	BCL9 and C9orf5 are associated with negative symptoms in schizophrenia: meta-analysis of two genome-wide association studies.	Schizophrenia (negative symptoms)	1	1	1	1
rs795544	1E-6	6	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs13207034	1E-6	6	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA-5-HIAA Factor score)	1	1	1	1
rs17834666	1E-6	6	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs62458065	1E-6	6	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs1902272	1E-6	6	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs6628506	1E-6	6	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	NA	NA	NA	NA
rs62287976	1E-6	6	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs421379	1E-6	6	23319801	Identification of inherited genetic variations influencing prognosis in early-onset breast cancer.	Breast cancer (prognosis)	1	1	1	1
rs6857	1E-6	6	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	0	1	1
rs2075650	1E-6	6	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	0	0	0
rs7676999	1E-6	6	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	1	1	1	1
rs6499100	1E-6	6	23297363	Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.	Tetralogy of Fallot	1	1	1	1
rs10048158	1E-6	6	23279374	Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain.	β2-Glycoprotein I (β2-GPI) plasma levels	0	0	0	0
rs2319125	1E-6	6	23279374	Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain.	β2-Glycoprotein I (β2-GPI) plasma levels	0	0	0	0
rs13287980	1E-6	6	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Gout	1	1	1	1
rs4149178	1E-6	6	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs2027760   	1E-6	6	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	NA	NA	NA	NA
rs12098973	1E-6	6	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	1	1	1	1
rs222054	1E-6	6	23213074	Association between liver-specific gene polymorphisms and their expression levels with nonalcoholic fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	0	1	1	1
rs17206232	1E-6	6	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	1	1	1	1
rs1920592	1E-6	6	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	0	1	1	1
rs2823743	1E-6	6	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	1	1	1	1
rs7953249	1E-6	6	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	1	1	1
rs11638815	1E-6	6	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity change in response to statin therapy	1	1	1	1
rs288139	1E-6	6	23118974	Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations.	Eye color	1	1	1	1
rs11710433	1E-6	6	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	1	1	1	1
rs931608	1E-6	6	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	0	1	1	1
rs11166135	1E-6	6	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs7634528	1E-6	6	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs1559777	1E-6	6	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs2238151	1E-6	6	23041239	Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.	Stroke (ischemic)	0	1	1	1
rs903263	1E-6	6	23001122	Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk.	Breast cancer (male) 	1	1	1	1
rs11698685	1E-6	6	23028342	New susceptibility loci associated with kidney disease in type 1 diabetes.	Type 1 diabetes nephropathy	0	1	1	1
rs1971791	1E-6	6	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	1	1	1	1
rs2364403	1E-6	6	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis (age of onset)	0	1	1	1
rs10030601	1E-6	6	22949513	Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32	Epilepsy (generalized)	1	1	1	1
rs4145462	1E-6	6	22881374	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	Alzheimer's disease (late onset)	1	1	1	1
rs11983798	1E-6	6	22881374	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	Alzheimer's disease (late onset)	1	1	1	1
rs6468852	1E-6	6	22881374	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	Alzheimer's disease (late onset)	1	1	1	1
rs10429924	1E-6	6	22885689	Genome-wide association study of multiplex schizophrenia pedigrees.	Schizophrenia	1	1	1	1
rs3847375	1E-6	6	22885689	Genome-wide association study of multiplex schizophrenia pedigrees.	Schizophrenia	1	1	1	1
rs1953600	1E-6	6	22936702	Genome-wide association analysis reveals 12q13.3-q14.1 as new risk locus for sarcoidosis.	Sarcoidosis	0	1	1	1
rs11742570	1E-6	6	22936669	A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.	Crohn's disease	0	0	1	1
rs10952132	1E-6	6	22890011	Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate.	Response to fenofibrate	1	1	1	1
rs13542	1E-6	6	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs813218	1E-6	6	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	0	1	1	1
rs10759102	1E-6	6	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs13144621	1E-6	6	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs7059886	1E-6	6	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	NA	NA	NA	NA
rs294588	1E-6	6	22773346	Linkage and association of successful aging to the 6q25 region in large Amish kindreds.	Aging	1	1	1	1
rs6925255	1E-6	6	22773346	Linkage and association of successful aging to the 6q25 region in large Amish kindreds.	Aging	1	1	1	1
rs295137	1E-6	6	22792082	Genome-wide association analysis in asthma subjects identifies SPATS2L as a novel bronchodilator response gene.	Asthma (bronchodilator response)	1	1	1	1
rs6646773	1E-6	6	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	NA	NA	NA	NA
rs6040399	1E-6	6	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	0	0	0	0
rs11935103	1E-6	6	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	1	1	1	1
rs1417066	1E-6	6	22763110	Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study.	Osteoarthritis	0	1	1	1
rs6575353	1E-6	6	22754043	A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.	Insomnia (caffeine-induced)	1	1	1	1
rs12032672	1E-6	6	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	1	1	1	1
rs1932040	1E-6	6	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	1	1	1	1
rs6885116	1E-6	6	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	1	1	1	1
rs4665972	1E-6	6	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	0	1	1	1
rs17356907	1E-6	6	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	0	1	1	1
rs9332739	1E-6	6	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (GA)	0	0	0	0
rs2054399	1E-6	6	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs6756590	1E-6	6	22683712	Genome-wide association analysis identifies susceptibility loci for migraine without aura.	Migraine	1	1	1	1
rs3916765	1E-6	6	22693455	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.	Type 2 diabetes	0	1	1	1
rs7230711	1E-6	6	22658931	A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed.	Immune response to anthrax vaccine 	1	1	1	1
rs12808148	1E-6	6	22832961	Genome-wide association study of Alzheimer's disease.	Alzheimer's disease	1	1	1	1
rs3820201	1E-6	6	22745009	Multiple loci influencing hippocampal degeneration identified by genome scan.	Hippocampal atrophy	1	1	1	1
rs959695	1E-6	6	22745009	Multiple loci influencing hippocampal degeneration identified by genome scan.	Hippocampal atrophy	1	1	1	1
rs11139399	1E-6	6	22745009	Multiple loci influencing hippocampal degeneration identified by genome scan.	Hippocampal atrophy	1	1	1	1
rs6754640	1E-6	6	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	1	1	1	1
rs7617219	1E-6	6	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs11154271	1E-6	6	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs7245708	1E-6	6	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs11725509	1E-6	6	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs2336030	1E-6	6	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs8106493	1E-6	6	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs11930273	1E-6	6	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs2798334	1E-6	6	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs7956193	1E-6	6	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs11712655	1E-6	6	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs1567127	1E-6	6	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs12316797	1E-6	6	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs4856162	1E-6	6	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	0	0	0	0
rs1397924	1E-6	6	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	0	0	0	0
rs7628767	1E-6	6	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	0	0	0	0
rs4493441	1E-6	6	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	0	0	0	0
rs4902960	1E-6	6	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	1	1	1	1
rs2250149	1E-6	6	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (feminism/equality)	1	1	1	1
rs8083633	1E-6	6	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (time)	1	1	1	1
rs11051970	1E-6	6	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	1	1	1	1
rs4833407	1E-6	6	22484627	A genome-wide association meta-analysis identifies new childhood obesity loci.	Obesity	1	1	1	1
rs948426	1E-6	6	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	1	1	1	1
rs7732320	1E-6	6	22472174	SSBP2 variants are associated with survival in glioblastoma patients.	Glioblastoma	1	1	1	1
rs2967951	1E-6	6	22446040	A novel locus for body mass index on 5p15.2: a meta-analysis of two genome-wide association studies.	Body mass index	1	1	1	1
rs1937395	1E-6	6	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs10875595	1E-6	6	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs275380	1E-6	6	22379998	Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.	Adverse response to lamotrigine and phenytoin	1	1	1	1
rs3853240	1E-6	6	22379998	Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.	Adverse response to lamotrigine and phenytoin	1	1	1	1
rs1296028	1E-6	6	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	0	1	1	1
rs10877840	1E-6	6	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	1	1	1	1
rs10519131	1E-6	6	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	1	1	1	1
rs1550404	1E-6	6	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	1	1	1	1
rs11986414	1E-6	6	22388998	Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation.	Gaucher disease severity	1	1	1	1
rs11661856	1E-6	6	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs17556665	1E-6	6	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs12220898	1E-6	6	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs11906160	1E-6	6	22216198	A genome-wide association study of the Protein C anticoagulant pathway.	Anticoagulant levels	0	0	0	0
rs7000782	1E-6	6	22197932	Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis.	Atopic dermatitis	1	1	1	1
rs2900174	1E-6	6	22142827	A genome-wide association study of overall survival in pancreatic cancer patients treated with gemcitabine in CALGB 80303.	Response to gemcitabine in pancreatic cancer 	1	1	1	1
rs921231	1E-6	6	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	1	1	1	1
rs7523050	1E-6	6	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	1	1	1	1
rs10789491	1E-6	6	22095909	Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.	Response to hepatitis C treatment	1	1	1	1
rs10776934	1E-6	6	22095909	Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.	Response to hepatitis C treatment	1	1	1	1
rs11858836	1E-6	6	22080838	A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13.	Chronic obstructive pulmonary disease	0	0	1	1
rs3942852	1E-6	6	22076464	Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	0	1	1	1
rs7156960	1E-6	6	22076464	Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs207954	1E-6	6	22076464	Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs573332	1E-6	6	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	NA	NA	NA	NA
rs7015622	1E-6	6	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	NA	NA	NA	NA
rs10744391	1E-6	6	22044751	Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study.	Renal sinus fat 	1	1	1	1
rs1044573	1E-6	6	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	Allergic rhinitis	0	1	1	1
rs6898653	1E-6	6	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	Allergic rhinitis	1	1	1	1
rs887864	1E-6	6	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	Allergic rhinitis	0	1	1	1
rs2069772	1E-6	6	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	IgE grass sensitization	0	1	1	1
rs5016282	1E-6	6	22012869	Genome-wide association study in German patients with attention deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	NA	NA	NA	NA
rs6430585	1E-6	6	21979947	A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.	Corneal structure	1	1	1	1
rs548181	1E-6	6	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	0	1	1
rs17512836	1E-6	6	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	0	1	1
rs2070615	1E-6	6	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	1	1	1	1
rs13139571	1E-6	6	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	0	1	0	0
rs37369	1E-6	6	21931564	A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection.	Metabolite levels	0	1	1	1
rs205611	1E-6	6	21835309	GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development.	Iris characteristics	1	1	1	1
rs11630290	1E-6	6	21835309	GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development.	Iris characteristics	1	1	1	1
rs8112449	1E-6	6	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs233100	1E-6	6	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs7255066	1E-6	6	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs4686760	1E-6	6	21810271	Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.	vWF and FVIII levels	1	1	1	1
rs379440	1E-6	6	21810271	Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.	vWF and FVIII levels	1	1	1	1
rs6708166	1E-6	6	21810271	Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.	vWF and FVIII levels	1	1	1	1
rs1425609	1E-6	6	21782286	A genome-wide association study of aging.	Aging (time to death)	1	1	1	1
rs12540874	1E-6	6	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	1	1	1
rs12575642	1E-6	6	21784300	Genome-wide association study of the child behavior checklist dysregulation profile.	Attention deficit hyperactivity disorder	0	1	1	1
rs10781500	1E-6	6	21743469	Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.	Ankylosing spondylitis	0	1	1	1
rs2056626	1E-6	6	21750679	Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.	Systemic sclerosis	0	0	1	1
rs12618769	1E-6	6	21738484	Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes.	Bipolar disorder	1	1	1	1
rs750338	1E-6	6	21703634	A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence.	Alcohol dependence	1	1	1	1
rs16872085	1E-6	6	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs13022357	1E-6	6	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs2715148	1E-6	6	21621269	Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples.	Major depressive disorder	1	1	1	1
rs2731672	1E-6	6	21546496	Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children.	Platelet function and related traits	0	1	1	1
rs7524102	1E-6	6	21533022	Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.	Bone mineral density	0	0	0	0
rs2774920	1E-6	6	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	1	1	1	1
rs16871023	1E-6	6	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	1	1	1	1
rs738322	1E-6	6	21478494	Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk.	Cutaneous nevi	0	0	1	1
rs2240466	1E-6	6	21490707	Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.	Caffeine consumption	0	1	1	1
rs987710	1E-6	6	21483845	Genome-wide association study identifies genetic loci associated with iron deficiency.	Iron deficiency	0	1	0	0
rs987710	1E-6	6	21483845	Genome-wide association study identifies genetic loci associated with iron deficiency.	Iron status biomarkers	0	0	0	0
rs17404956	1E-6	6	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs7296262	1E-6	6	21423239	A genome-wide association study of attempted suicide.	Suicide attempts in bipolar disorder	1	1	1	1
rs7808424	1E-6	6	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	1	1	1	1
rs4956211	1E-6	6	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	1	1	1	1
rs411174	1E-6	6	21368711	Genome-wide association study of personality traits in bipolar patients.	Personality dimensions	1	1	1	1
rs2934442	1E-6	6	21305692	Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder.	Bipolar disorder (age of onset and psychomotor symptoms)	1	1	1	1
rs3761218	1E-6	6	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs914715	1E-6	6	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	0	1	1	1
rs10134944	1E-6	6	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs1484170	1E-6	6	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	1	1	1	1
rs12907914	1E-6	6	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	1	1	1	1
rs7219585	1E-6	6	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs2121433	1E-6	6	21123754	Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort.	Alzheimer's disease biomarkers	1	1	1	1
rs157580	1E-6	6	21123754	Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort.	Alzheimer's disease biomarkers	0	1	1	1
rs429358	1E-6	6	21123754	Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort.	Alzheimer's disease biomarkers	0	0	1	1
rs439401	1E-6	6	21123754	Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort.	Alzheimer's disease biomarkers	0	0	0	0
rs7364180	1E-6	6	21123754	Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort.	Alzheimer's disease biomarkers	1	1	1	1
rs4499362	1E-6	6	21123754	Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort.	Alzheimer's disease biomarkers	0	0	0	0
rs2075650	1E-6	6	21123754	Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort.	Alzheimer's disease biomarkers	0	0	0	0
rs4703129	1E-6	6	21182207	Variants in several genomic regions associated with asperger disorder.	Asperger disorder	1	1	1	1
rs854384	1E-6	6	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	MRI atrophy measures	1	1	1	1
rs2852894	1E-6	6	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	MRI atrophy measures	1	1	1	1
rs17108533	1E-6	6	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Reasoning	1	1	1	1
rs2286720	1E-6	6	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Reasoning	1	1	1	1
rs17706989	1E-6	6	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Reasoning	1	1	1	1
rs3753242	1E-6	6	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Reasoning	1	1	1	1
rs17689437	1E-6	6	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Reasoning	0	1	1	1
rs7770731	1E-6	6	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Working memory	1	1	1	1
rs11710077	1E-6	6	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	1	1	1	1
rs12491921	1E-6	6	21668797	A genome-wide association study of DSM-IV cannabis dependence.	Cannabis dependence	1	1	1	1
rs12446956	1E-6	6	21042317	Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned.	Major depressive disorder	1	1	1	1
rs11554257	1E-6	6	20848476	Genetic predictors of medically refractory ulcerative colitis.	Ulcerative colitis	1	1	1	1
rs12580100	1E-6	6	20953189	Genome-wide association analysis identifies three psoriasis susceptibility loci.	Psoriasis	0	0	1	1
rs255414	1E-6	6	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	0	1	1	1
rs1727638	1E-6	6	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	AB1-42	1	1	1	1
rs7631605	1E-6	6	20932310	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	P-tau181p	1	1	1	1
rs6627057	1E-6	6	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	NA	NA	NA	NA
rs7727102	1E-6	6	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs7248363	1E-6	6	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs6024905	1E-6	6	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs11740562	1E-6	6	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs12282742	1E-6	6	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs17069122	1E-6	6	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1806864	1E-6	6	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs2018368	1E-6	6	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs2841307	1E-6	6	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs993804	1E-6	6	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs2078267	1E-6	6	20884846	Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.	Urate levels	0	0	0	0
rs9303542	1E-6	6	20852632	A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.	Ovarian cancer	0	0	1	1
rs10490775	1E-6	6	20825314	E2-2 protein and Fuchs's corneal dystrophy.	Fuchs's corneal dystrophy	1	1	1	1
rs127430	1E-6	6	20838585	Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.	Cardiovascular disease risk factors	1	1	1	1
rs2031577	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs6489785	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	0	1	1	1
rs3847687	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs4891159	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs10445407	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	0	1	1	1
rs4745062	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs2024714	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs7315621	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs16975963	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs4732038	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs2516739	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs7874142	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs4468878	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs13008689	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs2273	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs2882281	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs2282032	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs9876781	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs6568433	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs9517320	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	0	1	1	1
rs4148546	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs9592783	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs739401	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs10256972	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs3212335	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs6915183	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs4721135	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	0	1	1	1
rs3106598	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs1356888	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs9616906	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs13053175	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	0	1	1	1
rs5766691	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs13118159	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	0	1	1	1
rs7168365	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs7493138	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs432203	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs6813479	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs1327533	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs2826891	1E-6	6	20834067	Joint influence of small-effect genetic variants on human longevity.	Longevity	1	1	1	1
rs199533	1E-6	6	20711177	Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.	Parkinson's disease	0	0	1	1
rs6487679	1E-6	6	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (AST)	1	1	1	1
rs643608	1E-6	6	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs669408	1E-6	6	20694011	Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.	Immunoglobulin A 	1	1	1	1
rs1464807	1E-6	6	20732625	Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	1	1	1	1
rs7713917	1E-6	6	20673876	Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression.	Major depressive disorder	1	1	1	1
rs4965121	1E-6	6	20634892	A genome-wide association study of neuroticism in a population-based sample.	Neuroticism	1	1	1	1
rs3780792	1E-6	6	20598377	Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis.	Multiple sclerosis	NA	NA	NA	NA
rs3745672	1E-6	6	20598377	Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs11465804	1E-6	6	20570966	Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.	Crohn's disease	0	0	1	1
rs7940646	1E-6	6	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	1	1	1	1
rs12367822	1E-6	6	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	0	1	1	1
rs2601828	1E-6	6	20522523	Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.	Partial epilepsies	1	1	1	1
rs8074751	1E-6	6	20732626	Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	1	1	1	1
rs1520832	1E-6	6	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	1	1	1	1
rs4528684	1E-6	6	20400778	Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.	Mortality among heart failure patients	1	1	1	1
rs2125623	1E-6	6	20400778	Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.	Mortality among heart failure patients	1	1	1	1
rs11755724	1E-6	6	20385826	Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).	Age-related macular degeneration	0	1	1	1
rs10458787	1E-6	6	20397748	Genome-wide association study of height and body mass index in Australian twin families.	Body mass index	1	1	1	1
rs17082664	1E-6	6	20351715	Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.	Bipolar disorder and major depressive disorder (combined)	0	1	1	1
rs11773103	1E-6	6	20351715	Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.	Bipolar disorder and major depressive disorder (combined)	1	1	1	1
rs12912251	1E-6	6	20351715	Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.	Bipolar disorder and major depressive disorder (combined)	0	1	1	1
rs10746514	1E-6	6	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs12527253	1E-6	6	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs16909449	1E-6	6	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs10758669	1E-6	6	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	0	0	1	1
rs1986734	1E-6	6	20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Eosinophilic esophagitis (pediatric)	0	1	1	1
rs8056650	1E-6	6	20197096	Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.	Brain structure (hippocampal volume)	1	1	1	1
rs2074404	1E-6	6	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	0	1	1	1
rs2132683	1E-6	6	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs476463	1E-6	6	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs490592	1E-6	6	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs4534106	1E-6	6	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs2073233	1E-6	6	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs688872	1E-6	6	20171287	Voxelwise genome-wide association study (vGWAS).	Brain structure	1	1	1	1
rs2247572	1E-6	6	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs7151223	1E-6	6	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs270545	1E-6	6	20125088	Genome-wide association study of recurrent early-onset major depressive disorder.	Major depressive disorder	1	1	1	1
rs6537837	1E-6	6	20125088	Genome-wide association study of recurrent early-onset major depressive disorder.	Major depressive disorder	1	1	1	1
rs4837628	1E-6	6	20070850	Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.	Parkinson's disease	1	1	1	1
rs37062	1E-6	6	20062063	Several common variants modulate heart rate, PR interval and QRS duration.	Electrocardiographic traits	0	1	1	1
rs17151904	1E-6	6	20009918	A genome-wide association study of carotid atherosclerosis in HIV-infected men.	Carotid atherosclerosis in HIV infection	1	1	1	1
rs9870680	1E-6	6	20038947	Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.	Major depressive disorder (broad)	1	1	1	1
rs9468692	1E-6	6	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	0	1	1	1
rs16948255	1E-6	6	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	NA	NA	NA	NA
rs6751715	1E-6	6	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs12122100	1E-6	6	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs7756521	1E-6	6	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs1258763	1E-6	6	20023658	Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.	Orofacial clefts	0	1	1	1
rs7554511	1E-6	6	19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Ulcerative colitis	0	0	1	1
rs7349332	1E-6	6	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	0	1	1	1
rs7729273	1E-6	6	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs4668356	1E-6	6	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	0	1	1	1
rs1897031	1E-6	6	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs10888501	1E-6	6	19721433	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics.	Response to antipsychotic treatment	0	1	1	1
rs11626056	1E-6	6	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs748404	1E-6	6	19654303	Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.	Lung cancer	1	1	1	1
rs1926203	1E-6	6	19654303	Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.	Lung cancer	1	1	1	1
rs7728043	1E-6	6	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	QT interval	1	1	1	1
rs2650951	1E-6	6	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	QT interval	1	1	1	1
rs1348582	1E-6	6	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	QT interval	1	1	1	1
rs3117035	1E-6	6	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	0	1	1	1
rs1541010	1E-6	6	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs10514995	1E-6	6	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs2717128	1E-6	6	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs7318731	1E-6	6	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs1502844	1E-6	6	19571808	Common variants conferring risk of schizophrenia.	Schizophrenia	1	1	1	1
rs6726292	1E-6	6	19553259	Common body mass index-associated variants confer risk of extreme obesity.	Obesity (extreme)	1	1	1	1
rs999943	1E-6	6	19553259	Common body mass index-associated variants confer risk of extreme obesity.	Obesity (extreme)	0	1	1	1
rs8049603	1E-6	6	19525955	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.	Multiple sclerosis	1	1	1	1
rs6582630	1E-6	6	19483685	HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin.	Drug-induced liver injury (flucloxacillin)	0	1	1	1
rs10812428	1E-6	6	19483685	HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin.	Drug-induced liver injury (flucloxacillin)	1	1	1	1
rs4679904	1E-6	6	19458352	Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.	Primary biliary cirrhosis	1	1	1	1
rs10438933	1E-6	6	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs7577894	1E-6	6	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	0	1	1	1
rs11024074	1E-6	6	19430479	Genome-wide association study of blood pressure and hypertension.	Diastolic blood pressure	0	1	0	0
rs2242663	1E-6	6	19416921	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.	Bipolar disorder	0	0	1	1
rs10479002	1E-6	6	20031577	Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.	Fibrinogen	NA	NA	NA	NA
rs11254363	1E-6	6	19303062	Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations.	Folate pathway vitamin levels	0	0	1	1
rs17131547	1E-6	6	19249006	Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groups.	Bone mineral density	NA	NA	NA	NA
rs2416257	1E-6	6	19198610	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.	Eosinophil counts	0	1	1	1
rs17531088	1E-6	6	19132087	A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease.	Kawasaki disease	1	1	1	1
rs4598195	1E-6	6	19122664	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.	Ulcerative colitis	0	0	1	1
rs12046117	1E-6	6	19116933	Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis.	Arthritis (juvenile idiopathic)	1	1	1	1
rs2718812	1E-6	6	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	0	0	0
rs4516970	1E-6	6	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	1	1	1	1
rs2710057	1E-6	6	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (hip)	NA	NA	NA	NA
rs7336332	1E-6	6	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	1	1	1
rs1973993	1E-6	6	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	1	1	1
rs10769908	1E-6	6	19079261	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.	Body mass index	0	0	1	1
rs522958	1E-6	6	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	0	1	0	0
rs41441749	1E-6	6	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Hyperactive-impulsive symptoms	1	1	1	1
rs9523762	1E-6	6	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs10492664	1E-6	6	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs3757247	1E-6	6	18840781	Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.	Type 1 diabetes	0	0	1	1
rs2677744	1E-6	6	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	0	1	1	1
rs1934951	1E-6	6	18594024	Bisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysis.	Osteonecrosis of the jaw	0	1	1	1
rs2900976	1E-6	6	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs169082	1E-6	6	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs9402515	1E-6	6	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs6930337	1E-6	6	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs1285407	1E-6	6	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs2237878	1E-6	6	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	1	1	1
rs1939992	1E-6	6	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs10466868	1E-6	6	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs3018362	1E-6	6	18445777	Multiple genetic loci for bone mineral density and fractures.	Bone mineral density (hip)	0	1	1	1
rs1052483	1E-6	6	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs749052	1E-6	6	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs7249094	1E-6	6	18391951	Many sequence variants affecting diversity of adult human height.	Height	1	1	1	1
rs7869550	1E-6	6	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	0	0	1	1
rs11064768	1E-6	6	18332876	A genome-wide association study in 574 schizophrenia trios using DNA pooling.	Schizophrenia	1	1	1	1
rs1859962	1E-6	6	18264097	Multiple newly identified loci associated with prostate cancer susceptibility.	Prostate cancer	0	0	1	1
rs724016	1E-6	6	18193045	Common variants in the GDF5-UQCC region are associated with variation in human height.	Height	0	0	1	1
rs17532515	1E-6	6	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	NA	NA	NA	NA
rs1998303	1E-6	6	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	1	1	1	1
rs10489849	1E-6	6	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	0	0	0	0
rs10518765	1E-6	6	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	1	1	1	1
rs2387326	1E-6	6	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	1	1	1	1
rs1119582	1E-6	6	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	NA	NA	NA	NA
rs10485165	1E-6	6	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	1	1	1	1
rs2165468	1E-6	6	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Bone mineral density	1	1	1	1
rs10506701	1E-6	6	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Bone mineral density	1	1	1	1
rs4811196	1E-6	6	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Bone mineral density	1	1	1	1
rs1978503	1E-6	6	17903305	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	Breast cancer	1	1	1	1
rs2390582	1E-6	6	17903303	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	Coronary artery calcification	1	1	1	1
rs2179965	1E-6	6	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Cognitive test performance	1	1	1	1
rs3867498	1E-6	6	17903307	Framingham Heart Study genome-wide association: results for pulmonary function measures.	Pulmonary function	1	1	1	1
rs1160297	1E-6	6	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs17465637	1E-6	6	17634449	Genomewide association analysis of coronary artery disease.	Coronary heart disease	0	0	1	1
rs743777	1E-6	6	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Rheumatoid arthritis	1	1	1	1
rs564398	1E-6	6	17463249	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.	Type 2 diabetes	0	1	1	1
rs5743289	1E-6	6	17447842	Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.	Crohn's disease	0	0	1	1
rs9596905	2E-6	5.69897000433602	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	1	1	1	1
rs1007190	2E-6	5.69897000433602	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	1	1	1	1
rs1004689	2E-6	5.69897000433602	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	NA	NA	NA	NA
rs11174478	2E-6	5.69897000433602	23728906	A genome-wide association study of sleep habits and insomnia.	Insomnia	0	1	1	1
rs2725544	2E-6	5.69897000433602	23728906	A genome-wide association study of sleep habits and insomnia.	Insomnia	0	1	1	1
rs17737465	2E-6	5.69897000433602	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep duration	0	1	1	1
rs12153606	2E-6	5.69897000433602	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Cu levels)	1	1	1	1
rs6692700	2E-6	5.69897000433602	23698163	Genome-wide association study of serum selenium concentrations.	Serum selenium levels	1	1	1	1
rs6107853	2E-6	5.69897000433602	23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Body mass index	0	1	1	1
rs11847697	2E-6	5.69897000433602	23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Body mass index	0	0	1	1
rs1321847	2E-6	5.69897000433602	23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Body mass index	1	1	1	1
rs6764623	2E-6	5.69897000433602	23650146	A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Venous thromboembolism	1	1	1	1
rs6503782	2E-6	5.69897000433602	23577725	Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.	Age-related macular degeneration	1	1	1	1
rs1549309	2E-6	5.69897000433602	23636237	Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake.	Dietary macronutrient intake	1	1	1	1
rs6496044	2E-6	5.69897000433602	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	0	1	1	1
rs11083475	2E-6	5.69897000433602	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs12960119	2E-6	5.69897000433602	23585552	Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.	Rhegmatogenous retinal detachment	1	1	1	1
rs76765968	2E-6	5.69897000433602	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	1	1	1	1
rs117096873	2E-6	5.69897000433602	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs985795	2E-6	5.69897000433602	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs111383589	2E-6	5.69897000433602	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs1556640	2E-6	5.69897000433602	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs3120667	2E-6	5.69897000433602	23568457	Genetic variants associated with disordered eating.	Eating disorders	1	1	1	1
rs2115200	2E-6	5.69897000433602	23568457	Genetic variants associated with disordered eating.	Eating disorders	1	1	1	1
rs10175070	2E-6	5.69897000433602	23568457	Genetic variants associated with disordered eating.	Eating disorders (purging via substances) 	1	1	1	1
rs6001930	2E-6	5.69897000433602	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	0	0	1	1
rs2033654	2E-6	5.69897000433602	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (non-asthmatics)	0	1	1	1
rs2326017	2E-6	5.69897000433602	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (non-asthmatics)	0	0	0	0
rs12203592	2E-6	5.69897000433602	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Sunburns	0	1	0	0
rs7141276	2E-6	5.69897000433602	23555300	Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis.	Response to anti-TNF treatment in rheumatoid arthritis	1	1	1	1
rs6427528	2E-6	5.69897000433602	23555300	Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis.	Response to anti-TNF treatment in rheumatoid arthritis	1	1	1	1
rs78022502	2E-6	5.69897000433602	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs77636885	2E-6	5.69897000433602	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs75253868	2E-6	5.69897000433602	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs17301739	2E-6	5.69897000433602	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	0	1	1	1
rs7245858	2E-6	5.69897000433602	23535033	Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.	Alzheimer's disease (cognitive decline)	1	1	1	1
rs724767	2E-6	5.69897000433602	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs11548323	2E-6	5.69897000433602	23518928	TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.	Estradiol plasma levels (breast cancer)	1	1	1	1
rs16966122	2E-6	5.69897000433602	23496005	Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study.	Narcolepsy with cataplexy	1	1	1	1
rs2426087	2E-6	5.69897000433602	23496005	Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study.	Narcolepsy with cataplexy	1	1	1	1
rs8056064	2E-6	5.69897000433602	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs10180663	2E-6	5.69897000433602	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	0	1	1	1
rs6800901	2E-6	5.69897000433602	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs12638862	2E-6	5.69897000433602	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	0	1	1	1
rs2086824	2E-6	5.69897000433602	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs13028485	2E-6	5.69897000433602	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs1352075	2E-6	5.69897000433602	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (hyperdiploidy)	1	1	1	1
rs2677780	2E-6	5.69897000433602	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Smooth-surface caries 	0	1	1	1
rs2010809	2E-6	5.69897000433602	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Smooth-surface caries 	1	1	1	1
rs1079204	2E-6	5.69897000433602	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Smooth-surface caries 	1	1	1	1
rs3596	2E-6	5.69897000433602	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	0	0	1	1
rs7006687	2E-6	5.69897000433602	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	0	1	1	1
rs6755560	2E-6	5.69897000433602	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	1	1	1	1
rs11225148	2E-6	5.69897000433602	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs12122440	2E-6	5.69897000433602	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	1	1	1	1
rs17541203	2E-6	5.69897000433602	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	1	1	1	1
rs2090409	2E-6	5.69897000433602	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs6602217	2E-6	5.69897000433602	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs249954	2E-6	5.69897000433602	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs10860392	2E-6	5.69897000433602	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs6867265	2E-6	5.69897000433602	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs609412	2E-6	5.69897000433602	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs2297909	2E-6	5.69897000433602	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs6990255	2E-6	5.69897000433602	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs9834970	2E-6	5.69897000433602	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs1978968	2E-6	5.69897000433602	23509613	Genome-wide association study of antiphospholipid antibodies.	Presence of antiphospholipid antibodies	0	1	1	1
rs10492418	2E-6	5.69897000433602	23509613	Genome-wide association study of antiphospholipid antibodies.	Presence of antiphospholipid antibodies	1	1	1	1
rs9324268	2E-6	5.69897000433602	23432519	A genome-wide association study of recipient genotype and medium-term kidney allograft function.	Renal transplant outcome	1	1	1	1
rs7039300	2E-6	5.69897000433602	23419831	APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.	Alzheimer's disease biomarkers	1	1	1	1
rs11026091	2E-6	5.69897000433602	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs4804416	2E-6	5.69897000433602	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs1501550	2E-6	5.69897000433602	23381795	Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1.	Circulating vasoactive peptide levels 	1	1	1	1
rs12611334	2E-6	5.69897000433602	23894747	A comprehensive family-based replication study of schizophrenia genes.	Schizophrenia	1	1	1	1
rs9601248	2E-6	5.69897000433602	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs10065906	2E-6	5.69897000433602	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	0	0	0	0
rs12513663	2E-6	5.69897000433602	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs10174573	2E-6	5.69897000433602	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs1034394	2E-6	5.69897000433602	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs1525293	2E-6	5.69897000433602	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs1107366	2E-6	5.69897000433602	23378610	Genetic variants associated with glycine metabolism and their role in insulin sensitivity and type 2 diabetes.	Metabolite levels	1	1	1	1
rs459482	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs17776120	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs586446	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9574309	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1467979	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6908917	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2659005	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7734985	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11847263	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs17515642	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4650376	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10758189	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs3793039	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7072055	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6853847	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs12580240	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6102185	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6466479	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs8076431	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11820502	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs846271	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs909674	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11169838	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs6687262	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11710456	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2514895	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7111562	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2060070	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1054052	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4779031	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11199254	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9948784	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs3097645	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7731390	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9308433	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6794649	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2389339	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs13272623	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs308097	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4832928	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs5764106	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs13272236	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs16884711	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6479779	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10861342	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs9403856	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs11763760	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs626657	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9886428	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2887004	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7159888	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs5771040	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs12455580	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2745851	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs16871226	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs17348299	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2072209	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7582701	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs9468811	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10508459	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2919856	2E-6	5.69897000433602	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs17636071	2E-6	5.69897000433602	23374588	Pharmacogenomics in Alzheimer's disease: a genome-wide association study of response to cholinesterase inhibitors.	Response to cholinesterase inhibitors in Alzheimer's disease	1	1	1	1
rs1931575 	2E-6	5.69897000433602	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	NA	NA	NA	NA
rs788076 	2E-6	5.69897000433602	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	NA	NA	NA	NA
rs12587252 	2E-6	5.69897000433602	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	NA	NA	NA	NA
rs2860223	2E-6	5.69897000433602	23382809	BCL9 and C9orf5 are associated with negative symptoms in schizophrenia: meta-analysis of two genome-wide association studies.	Schizophrenia (negative symptoms)	1	1	1	1
rs8180040	2E-6	5.69897000433602	23350875	A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12.	Colorectal cancer	1	1	1	1
rs16882214	2E-6	5.69897000433602	23354978	Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation.	Breast cancer	1	1	1	1
rs1078806	2E-6	5.69897000433602	23354978	Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation.	Breast cancer	0	0	1	1
rs2647046	2E-6	5.69897000433602	23349640	Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.	Lymphoma	0	0	0	0
rs12445126	2E-6	5.69897000433602	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs9445732	2E-6	5.69897000433602	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs11644988	2E-6	5.69897000433602	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs485842	2E-6	5.69897000433602	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	0	1	1	1
rs4409675	2E-6	5.69897000433602	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs13402855	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA)	1	1	1	1
rs79156074	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA/ MHPG Ratio)	1	1	1	1
rs68184094	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA)	1	1	1	1
rs3795958	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA)	1	1	1	1
rs6802119	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA)	NA	NA	NA	NA
rs187200046	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA)	1	1	1	1
rs13251954	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA-5-HIAA Factor score)	1	1	1	1
rs1881744	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/5-HIAA ratio)	1	1	1	1
rs112288323	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	0	1	0	0
rs2009501	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs9296949	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	0	1	1	1
rs62494762	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs8021963	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs12050794	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs34924084	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs72960926	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs11245052	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs5004866	2E-6	5.69897000433602	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	NA	NA	NA	NA
rs17586843	2E-6	5.69897000433602	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	0	0	0
rs6480975	2E-6	5.69897000433602	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	1	1	1	1
rs7646881	2E-6	5.69897000433602	23297363	Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.	Tetralogy of Fallot	0	1	1	1
rs4925295	2E-6	5.69897000433602	23279374	Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain.	β2-Glycoprotein I (β2-GPI) plasma levels	1	1	1	1
rs193741	2E-6	5.69897000433602	23279374	Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain.	β2-Glycoprotein I (β2-GPI) plasma levels	1	1	1	1
rs11190179	2E-6	5.69897000433602	23279374	Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain.	β2-Glycoprotein I (β2-GPI) plasma levels	1	1	1	1
rs39453	2E-6	5.69897000433602	23300701	Genome-wide search for gene-gene interactions in colorectal cancer.	Colorectal cancer	1	1	1	1
rs12955983	2E-6	5.69897000433602	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs2195525	2E-6	5.69897000433602	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs1571500	2E-6	5.69897000433602	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	0	0	1	1
rs775227	2E-6	5.69897000433602	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs13092825	2E-6	5.69897000433602	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	0	0	0	0
rs1383934	2E-6	5.69897000433602	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	0	0	0	0
rs2108258	2E-6	5.69897000433602	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs4251631	2E-6	5.69897000433602	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	0	0	0	0
rs1953743	2E-6	5.69897000433602	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs1198872	2E-6	5.69897000433602	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	1	1	1	1
rs11864146	2E-6	5.69897000433602	23213074	Association between liver-specific gene polymorphisms and their expression levels with nonalcoholic fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs7853844	2E-6	5.69897000433602	23180869	Genome-wide association study of survival in patients with pancreatic adenocarcinoma.	Pancreatic cancer	1	1	1	1
rs9951925	2E-6	5.69897000433602	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	1	1	1	1
rs652520	2E-6	5.69897000433602	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	1	1	1	1
rs10144042	2E-6	5.69897000433602	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity change in response to statin therapy	0	1	1	1
rs1392635	2E-6	5.69897000433602	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity change in response to statin therapy	1	1	1	1
rs4450798	2E-6	5.69897000433602	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	1	1	1	1
rs11773966	2E-6	5.69897000433602	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	1	1	1	1
rs10865974	2E-6	5.69897000433602	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	0	1	1	1
rs10111661	2E-6	5.69897000433602	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs848452	2E-6	5.69897000433602	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	0	1	1	1
rs1204798	2E-6	5.69897000433602	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	0	1	1	1
rs1750491	2E-6	5.69897000433602	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs11100904	2E-6	5.69897000433602	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	0	1	1	1
rs1229542	2E-6	5.69897000433602	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs1944866	2E-6	5.69897000433602	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs7215564	2E-6	5.69897000433602	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	0	1	1	1
rs9984974	2E-6	5.69897000433602	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	0	1	1	1
rs2675609	2E-6	5.69897000433602	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum total protein level	1	1	1	1
rs17837497	2E-6	5.69897000433602	23007406	Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	NA	NA	NA	NA
rs4871297	2E-6	5.69897000433602	23028342	New susceptibility loci associated with kidney disease in type 1 diabetes.	Type 1 diabetes nephropathy	1	1	1	1
rs614226	2E-6	5.69897000433602	23028342	New susceptibility loci associated with kidney disease in type 1 diabetes.	Type 1 diabetes nephropathy	1	1	1	1
rs7896691	2E-6	5.69897000433602	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs4917300	2E-6	5.69897000433602	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	1	1	1	1
rs6956741	2E-6	5.69897000433602	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis (age of onset)	1	1	1	1
rs7638995	2E-6	5.69897000433602	22881374	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	Alzheimer's disease (late onset)	1	1	1	1
rs9969729	2E-6	5.69897000433602	22881374	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	Alzheimer's disease (late onset)	0	1	1	1
rs2245641	2E-6	5.69897000433602	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	0	1	1	1
rs10995485	2E-6	5.69897000433602	22890011	Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate.	Response to fenofibrate	1	1	1	1
rs519595	2E-6	5.69897000433602	22890011	Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate.	Response to fenofibrate	1	1	1	1
rs1258763	2E-6	5.69897000433602	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	0	0	1	1
rs1373453	2E-6	5.69897000433602	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs5765956	2E-6	5.69897000433602	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs883924	2E-6	5.69897000433602	22841784	Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.	Hepatitis C induced liver fibrosis	1	1	1	1
rs7799265	2E-6	5.69897000433602	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs11766496	2E-6	5.69897000433602	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs9900808	2E-6	5.69897000433602	22823124	The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation.	Cannabis use (initiation)	1	1	1	1
rs7169523	2E-6	5.69897000433602	23055271	Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.	Myasthenia gravis 	1	1	1	1
rs2903308	2E-6	5.69897000433602	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	1	1	1	1
rs4502542	2E-6	5.69897000433602	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	NA	NA	NA	NA
rs6563353	2E-6	5.69897000433602	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	1	1	1	1
rs11935103	2E-6	5.69897000433602	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	0	0	0	0
rs7628219	2E-6	5.69897000433602	22754043	A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.	Insomnia (caffeine-induced)	1	1	1	1
rs10043775	2E-6	5.69897000433602	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	0	1	1	1
rs9942773	2E-6	5.69897000433602	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	1	1	1	1
rs1011108	2E-6	5.69897000433602	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	1	1	1	1
rs1360573	2E-6	5.69897000433602	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	1	1	1	1
rs10771431	2E-6	5.69897000433602	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	0	1	1	1
rs11919041	2E-6	5.69897000433602	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs13401620	2E-6	5.69897000433602	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	0	1	1	1
rs12585963	2E-6	5.69897000433602	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs722782	2E-6	5.69897000433602	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (GA)	NA	NA	NA	NA
rs836589	2E-6	5.69897000433602	22704111	Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.	Erectile dysfunction	1	1	1	1
rs10488084	2E-6	5.69897000433602	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Estradiol levels	1	1	1	1
rs1015657	2E-6	5.69897000433602	22648509	PKNOX2 is associated with formal thought disorder in schizophrenia: a meta-analysis of two genome-wide association studies.	Formal thought disorder in schizophrenia	1	1	1	1
rs11224899	2E-6	5.69897000433602	22648509	PKNOX2 is associated with formal thought disorder in schizophrenia: a meta-analysis of two genome-wide association studies.	Formal thought disorder in schizophrenia	1	1	1	1
rs10958605	2E-6	5.69897000433602	22658654	Genomic determinants of motor and cognitive outcomes in Parkinson's disease.	Parkinson's disease (motor and cognition)	1	1	1	1
rs13383928	2E-6	5.69897000433602	22637743	Genome-wide gene-environment interaction analysis for asbestos exposure in lung cancer susceptibility.	Lung cancer-asbestos exposure interaction	1	1	1	1
rs1031261	2E-6	5.69897000433602	22745009	Multiple loci influencing hippocampal degeneration identified by genome scan.	Hippocampal atrophy	1	1	1	1
rs17680945	2E-6	5.69897000433602	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	1	1	1	1
rs987360	2E-6	5.69897000433602	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	1	1	1	1
rs1494508	2E-6	5.69897000433602	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	0	1	1	1
rs1996720	2E-6	5.69897000433602	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	1	1	1	1
rs10849893	2E-6	5.69897000433602	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	1	1	1	1
rs7981942	2E-6	5.69897000433602	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	0	1	1	1
rs869834	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs17008402	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs2324999	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	0	1	1	1
rs7245708	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	0	0	0	0
rs12943829	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs9409154	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs12175489	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	0	1	1	1
rs12562437	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs4376189	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs17025426	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs12022722	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	0	0	0
rs10089517	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	1	1	1
rs7705033	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	1	1	1
rs10992471	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	1	1	1
rs10910018	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	0	1	0	0
rs7627289	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs3846635	2E-6	5.69897000433602	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs210648	2E-6	5.69897000433602	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	0	1	1	1
rs2291447	2E-6	5.69897000433602	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	0	1	1	1
rs574773	2E-6	5.69897000433602	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs7612581	2E-6	5.69897000433602	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	0	0	0	0
rs10511217	2E-6	5.69897000433602	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	0	0	0	0
rs12485744	2E-6	5.69897000433602	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	0	0	0	0
rs2250245	2E-6	5.69897000433602	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (feminism/equality)	0	0	0	0
rs4384209	2E-6	5.69897000433602	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (feminism/equality)	1	1	1	1
rs240768	2E-6	5.69897000433602	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	1	1	1	1
rs1346987	2E-6	5.69897000433602	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	1	1	1	1
rs12499086	2E-6	5.69897000433602	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (time)	1	1	1	1
rs11730243	2E-6	5.69897000433602	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (time)	0	0	0	0
rs11045392	2E-6	5.69897000433602	22569225	Investigation of single nucleotide polymorphisms and biological pathways associated with response to TNFα inhibitors in patients with rheumatoid arthritis.	Response to TNF-alpha inhibitors in rheumatoid arthritis	0	1	1	1
rs11745587	2E-6	5.69897000433602	22561531	Genome-wide association study to identify genetic determinants of severe asthma.	Asthma	0	0	1	1
rs2766692	2E-6	5.69897000433602	22554406	Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6.	Electroencephalographic traits in alcoholism	1	1	1	1
rs560887	2E-6	5.69897000433602	22508271	Fasting glucose GWAS candidate region analysis across ethnic groups in the Multiethnic Study of Atherosclerosis (MESA).	Fasting plasma glucose	0	0	1	1
rs4820255	2E-6	5.69897000433602	22509378	A genome-wide association study of female sexual dysfunction.	Sexual dysfunction (female)	1	1	1	1
rs2370759	2E-6	5.69897000433602	22509378	A genome-wide association study of female sexual dysfunction.	Sexual dysfunction (female)	1	1	1	1
rs4704397	2E-6	5.69897000433602	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	0	1	1	1
rs507506	2E-6	5.69897000433602	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	1	1	1	1
rs1902618	2E-6	5.69897000433602	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs10808265	2E-6	5.69897000433602	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs10104895	2E-6	5.69897000433602	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs7192208	2E-6	5.69897000433602	22425255	A genome-wide search for genetic influences and biological pathways related to the brain's white matter integrity.	White matter integrity	1	1	1	1
rs6990917	2E-6	5.69897000433602	22379998	Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.	Adverse response to lamotrigine and phenytoin	1	1	1	1
rs9919839	2E-6	5.69897000433602	22379998	Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.	Adverse response to lamotrigine and phenytoin	1	1	1	1
rs3936340	2E-6	5.69897000433602	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	1	1	1	1
rs240657	2E-6	5.69897000433602	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	1	1	1	1
rs6767049	2E-6	5.69897000433602	22365631	Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.	Temperament (bipolar disorder)	1	1	1	1
rs17599018	2E-6	5.69897000433602	22365631	Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.	Temperament (bipolar disorder)	1	1	1	1
rs17371334	2E-6	5.69897000433602	22365631	Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.	Temperament (bipolar disorder)	1	1	1	1
rs4698169	2E-6	5.69897000433602	22365631	Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.	Temperament (bipolar disorder)	1	1	1	1
rs82625	2E-6	5.69897000433602	22388998	Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation.	Gaucher disease severity	1	1	1	1
rs867186	2E-6	5.69897000433602	22443383	Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.	Hemostatic factors and hematological phenotypes	0	1	1	1
rs12999373	2E-6	5.69897000433602	22229870	Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia.	Uric acid levels	0	1	1	1
rs17460823	2E-6	5.69897000433602	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs11979476	2E-6	5.69897000433602	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs4909764	2E-6	5.69897000433602	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	NA	NA	NA	NA
rs9857275	2E-6	5.69897000433602	22210626	Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.	Prion diseases	0	1	1	1
rs3853601	2E-6	5.69897000433602	22197932	Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis.	Atopic dermatitis	0	1	1	1
rs502514	2E-6	5.69897000433602	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	0	1	1	1
rs921231	2E-6	5.69897000433602	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	0	0	0	0
rs10479469	2E-6	5.69897000433602	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	1	1	1	1
rs1495377	2E-6	5.69897000433602	22137330	Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.	Creutzfeldt-Jakob disease (variant)	0	1	1	1
rs12273350	2E-6	5.69897000433602	22137330	Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.	Creutzfeldt-Jakob disease (variant)	1	1	1	1
rs2504916	2E-6	5.69897000433602	22095909	Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.	Response to hepatitis C treatment	0	1	1	1
rs920590	2E-6	5.69897000433602	22076464	Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs9290877	2E-6	5.69897000433602	22075330	A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study.	IgE levels 	1	1	1	1
rs237899	2E-6	5.69897000433602	22064162	Genome-wide association study of comorbid depressive syndrome and alcohol dependence.	Depression and alcohol dependence	1	1	1	1
rs6795349	2E-6	5.69897000433602	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	NA	NA	NA	NA
rs491376	2E-6	5.69897000433602	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	NA	NA	NA	NA
rs2034588	2E-6	5.69897000433602	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	NA	NA	NA	NA
rs12157904	2E-6	5.69897000433602	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	1	1	1	1
rs16990008	2E-6	5.69897000433602	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	NA	NA	NA	NA
rs216518	2E-6	5.69897000433602	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	Allergic rhinitis	1	1	1	1
rs4724100	2E-6	5.69897000433602	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	Allergic rhinitis	1	1	1	1
rs631208	2E-6	5.69897000433602	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	IgE grass sensitization	1	1	1	1
rs6673480	2E-6	5.69897000433602	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	IgE grass sensitization	0	1	1	1
rs7638110	2E-6	5.69897000433602	22013104	Genome-wide scan for loci of adolescent obesity and their relationship with blood pressure.	Obesity and blood pressure	0	0	0	0
rs4980785	2E-6	5.69897000433602	22010048	A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23.	Renal cell carcinoma	1	1	1	1
rs2011905	2E-6	5.69897000433602	21993531	Genome-wide association study does not reveal major genetic determinants for anti-cytomegalovirus antibody response.	Cytomegalovirus antibody response	1	1	1	1
rs6001027	2E-6	5.69897000433602	21983787	Genome-wide association study identifies three new melanoma susceptibility loci.	Melanoma	0	0	1	1
rs6442925	2E-6	5.69897000433602	21979947	A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.	Corneal structure	1	1	1	1
rs1551943	2E-6	5.69897000433602	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs1722784	2E-6	5.69897000433602	21926416	Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.	Melanoma	0	0	1	1
rs4765905	2E-6	5.69897000433602	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	0	1	1
rs4775413	2E-6	5.69897000433602	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	0	1	1
rs11130874	2E-6	5.69897000433602	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	1	1	1
rs12699131	2E-6	5.69897000433602	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	1	1	1	1
rs3845817	2E-6	5.69897000433602	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	1	1	1	1
rs6746896	2E-6	5.69897000433602	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	0	0	1	1
rs736408	2E-6	5.69897000433602	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	0	0	1	1
rs12130212	2E-6	5.69897000433602	21935397	Genome-wide population-based association study of extremely overweight young adults--the GOYA study.	Obesity (extreme)	1	1	1	1
rs13082711	2E-6	5.69897000433602	21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Systolic blood pressure	0	1	0	0
rs6015450	2E-6	5.69897000433602	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	0	0	0
rs281380	2E-6	5.69897000433602	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs9321490	2E-6	5.69897000433602	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs1062158	2E-6	5.69897000433602	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs2872507	2E-6	5.69897000433602	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	1	1	1
rs743777	2E-6	5.69897000433602	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	1	1	1
rs1354492	2E-6	5.69897000433602	21810271	Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.	vWF and FVIII levels	1	1	1	1
rs4936894	2E-6	5.69897000433602	21782286	A genome-wide association study of aging.	Aging (time to death)	1	1	1	1
rs766903	2E-6	5.69897000433602	21782286	A genome-wide association study of aging.	Aging (time to death)	1	1	1	1
rs8099939	2E-6	5.69897000433602	21771265	Genome-wide association study on bipolar disorder in the Bulgarian population.	Bipolar disorder	1	1	1	1
rs7501939	2E-6	5.69897000433602	21743057	Genome-wide association study identifies new prostate cancer susceptibility loci.	Prostate cancer	0	0	1	1
rs17197037	2E-6	5.69897000433602	21738484	Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes.	Bipolar disorder	1	1	1	1
rs743777	2E-6	5.69897000433602	21653640	Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways.	Rheumatoid arthritis	0	0	1	1
rs944260	2E-6	5.69897000433602	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs11708189	2E-6	5.69897000433602	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs6660565	2E-6	5.69897000433602	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs17550532	2E-6	5.69897000433602	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs3864663	2E-6	5.69897000433602	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs13438327	2E-6	5.69897000433602	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs9883654	2E-6	5.69897000433602	21659360	Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial.	Response to antineoplastic agents	1	1	1	1
rs10958369	2E-6	5.69897000433602	21659360	Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial.	Response to antineoplastic agents	1	1	1	1
rs7565124	2E-6	5.69897000433602	21621269	Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples.	Major depressive disorder	1	1	1	1
rs8023445	2E-6	5.69897000433602	21621269	Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples.	Major depressive disorder	1	1	1	1
rs10491334	2E-6	5.69897000433602	21612516	Association study on long-living individuals from Southern Italy identifies rs10491334 in the CAMKIV gene that regulates survival proteins.	Longevity	1	1	1	1
rs1403543	2E-6	5.69897000433602	21602797	Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.	Cystic fibrosis severity	NA	NA	NA	NA
rs11239930	2E-6	5.69897000433602	21502085	Genome-wide association study implicates PARD3B-based AIDS restriction.	AIDS progression	0	1	1	1
rs16867321	2E-6	5.69897000433602	21552555	A genome-wide association study on obesity and obesity-related traits.	Obesity	1	1	1	1
rs2548145	2E-6	5.69897000433602	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (alcohol use disorder factor score)	1	1	1	1
rs9556711	2E-6	5.69897000433602	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (alcohol use disorder factor score)	0	1	0	0
rs2369955	2E-6	5.69897000433602	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (heaviness of drinking)	1	1	1	1
rs16861990	2E-6	5.69897000433602	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	0	1	1	1
rs16930685	2E-6	5.69897000433602	21478494	Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk.	Cutaneous nevi	1	1	1	1
rs621559	2E-6	5.69897000433602	21460395	A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer.	Telomere length	1	1	1	1
rs398652	2E-6	5.69897000433602	21460395	A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer.	Telomere length	1	1	1	1
rs10927101	2E-6	5.69897000433602	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	0	0	0	0
rs10403021	2E-6	5.69897000433602	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs1092913	2E-6	5.69897000433602	21424380	Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibility.	Breast cancer	0	1	1	1
rs7651039	2E-6	5.69897000433602	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	1	1	1	1
rs2431697	2E-6	5.69897000433602	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	1	1	1	1
rs5754217	2E-6	5.69897000433602	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	0	1	1	1
rs918959	2E-6	5.69897000433602	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	0	1	1	1
rs7795096	2E-6	5.69897000433602	21305692	Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder.	Bipolar disorder (age of onset and psychomotor symptoms)	1	1	1	1
rs2989476	2E-6	5.69897000433602	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	0	0	1	1
rs1375144	2E-6	5.69897000433602	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs4627791	2E-6	5.69897000433602	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs1568889	2E-6	5.69897000433602	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs11622475	2E-6	5.69897000433602	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs1344484	2E-6	5.69897000433602	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	0	1	1	1
rs7247513	2E-6	5.69897000433602	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs6995588	2E-6	5.69897000433602	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	1	1	1	1
rs10506410	2E-6	5.69897000433602	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	1	1	1	1
rs10510102	2E-6	5.69897000433602	21263130	Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study.	Breast cancer	1	1	1	1
rs1844437	2E-6	5.69897000433602	21302353	Genome-wide association study of hoarding traits.	Hoarding	1	1	1	1
rs2032794	2E-6	5.69897000433602	21173776	Meta-analysis of genome-wide association studies for personality.	Personality dimensions	1	1	1	1
rs10089	2E-6	5.69897000433602	21139019	A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum.	Ileal carcinoids	0	1	1	1
rs10490919	2E-6	5.69897000433602	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs2392362	2E-6	5.69897000433602	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs523340	2E-6	5.69897000433602	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs9378805	2E-6	5.69897000433602	21131588	Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL.	Chronic lymphocytic leukemia	0	0	1	1
rs927675	2E-6	5.69897000433602	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	MRI atrophy measures	1	1	1	1
rs1857353	2E-6	5.69897000433602	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	MRI atrophy measures	1	1	1	1
rs7517337	2E-6	5.69897000433602	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	1	1	1	1
rs9471576	2E-6	5.69897000433602	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	0	1	1	1
rs368331	2E-6	5.69897000433602	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	1	1	1	1
rs4670766	2E-6	5.69897000433602	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	1	1	1	1
rs263238	2E-6	5.69897000433602	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	1	1	1	1
rs1264202	2E-6	5.69897000433602	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Reasoning	1	1	1	1
rs16865258	2E-6	5.69897000433602	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Working memory	1	1	1	1
rs7359257	2E-6	5.69897000433602	21102462	Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.	Menarche (age at onset)	0	1	1	1
rs4698412	2E-6	5.69897000433602	21084426	Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.	Parkinson's disease	0	0	1	1
rs6959888	2E-6	5.69897000433602	21079607	A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.	Anorexia nervosa	1	1	1	1
rs17725255	2E-6	5.69897000433602	21079607	A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.	Anorexia nervosa	1	1	1	1
rs8065311	2E-6	5.69897000433602	21668797	A genome-wide association study of DSM-IV cannabis dependence.	Cannabis dependence	0	0	0	0
rs11764116	2E-6	5.69897000433602	20848476	Genetic predictors of medically refractory ulcerative colitis.	Ulcerative colitis	1	1	1	1
rs1956388	2E-6	5.69897000433602	20848476	Genetic predictors of medically refractory ulcerative colitis.	Ulcerative colitis	0	1	1	1
rs6955651	2E-6	5.69897000433602	20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Body mass index	1	1	1	1
rs11880706	2E-6	5.69897000433602	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs240444	2E-6	5.69897000433602	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	NA	NA	NA	NA
rs7512769	2E-6	5.69897000433602	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs6952808	2E-6	5.69897000433602	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs1107592	2E-6	5.69897000433602	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	0	0	0
rs252817	2E-6	5.69897000433602	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs5955415	2E-6	5.69897000433602	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	NA	NA	NA	NA
rs915071	2E-6	5.69897000433602	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs9377619	2E-6	5.69897000433602	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1558861	2E-6	5.69897000433602	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	LDL cholesterol	0	0	0	0
rs2084881	2E-6	5.69897000433602	20852632	A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.	Ovarian cancer	0	0	0	0
rs8074980	2E-6	5.69897000433602	20802204	Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis.	Multiple sclerosis--Brain Glutamate Levels	1	1	1	1
rs2038256	2E-6	5.69897000433602	20802204	Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis.	Multiple sclerosis--Brain Glutamate Levels	1	1	1	1
rs8070473	2E-6	5.69897000433602	20800221	Genome-wide association scan of trait depression.	Depression (quantitative trait)	1	1	1	1
rs349475	2E-6	5.69897000433602	20800221	Genome-wide association scan of trait depression.	Depression (quantitative trait)	1	1	1	1
rs1001021	2E-6	5.69897000433602	20713499	Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression.	Schizophrenia, bipolar disorder and depression (combined)	1	1	1	1
rs9292394	2E-6	5.69897000433602	20709820	Genome-wide association study identifies BICD1 as a susceptibility gene for emphysema.	Emphysema-related traits	1	1	1	1
rs2499604	2E-6	5.69897000433602	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (AST)	1	1	1	1
rs1414896	2E-6	5.69897000433602	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (AST)	1	1	1	1
rs9584805	2E-6	5.69897000433602	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (lobular)	0	1	1	1
rs4237591	2E-6	5.69897000433602	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (lobular)	1	1	1	1
rs4243849	2E-6	5.69897000433602	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs1529093	2E-6	5.69897000433602	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs11038871	2E-6	5.69897000433602	20694011	Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.	Immunoglobulin A 	0	1	1	1
rs12669076	2E-6	5.69897000433602	20694011	Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.	Immunoglobulin A 	0	1	1	1
rs7197653	2E-6	5.69897000433602	20700443	Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.	Magnesium levels	0	1	1	1
rs7567389	2E-6	5.69897000433602	20707712	A genome-wide association study of self-rated health.	Self-rated health	0	1	1	1
rs9310709	2E-6	5.69897000433602	20686651	Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases.	Chronic kidney disease and serum creatinine levels	1	1	1	1
rs13070584	2E-6	5.69897000433602	20686651	Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases.	Chronic kidney disease and serum creatinine levels	1	1	1	1
rs4430796	2E-6	5.69897000433602	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	0	1	1	1
rs6052699	2E-6	5.69897000433602	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	1	1	1	1
rs4947339	2E-6	5.69897000433602	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	0	1	1	1
rs1859156	2E-6	5.69897000433602	20732626	Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	1	1	1	1
rs4923705	2E-6	5.69897000433602	20732626	Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	1	1	1	1
rs840016	2E-6	5.69897000433602	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs10865035	2E-6	5.69897000433602	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	0	0	0
rs4750316	2E-6	5.69897000433602	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs17374222	2E-6	5.69897000433602	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs4298437	2E-6	5.69897000433602	20452100	Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study.	Alzheimer's disease	1	1	1	1
rs17019682	2E-6	5.69897000433602	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	1	1	1	1
rs1975174	2E-6	5.69897000433602	20421499	Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology.	Telomere length	0	0	1	1
rs4452212	2E-6	5.69897000433602	20421499	Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology.	Telomere length	0	1	1	1
rs7965445	2E-6	5.69897000433602	20400778	Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.	Mortality among heart failure patients	1	1	1	1
rs6868223	2E-6	5.69897000433602	20400778	Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.	Mortality among heart failure patients	1	1	1	1
rs2898681	2E-6	5.69897000433602	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (cup)	1	1	1	1
rs1884537	2E-6	5.69897000433602	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (disc)	1	1	1	1
rs9488363	2E-6	5.69897000433602	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (rim)	1	1	1	1
rs2958154	2E-6	5.69897000433602	20385819	Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.	Age-related macular degeneration	0	1	1	1
rs6594713	2E-6	5.69897000433602	20308991	Integrative genome-wide association analysis of cytoarchitectural abnormalities in the prefrontal cortex of psychiatric disorders.	Brain cytoarchitecture	1	1	1	1
rs11893063	2E-6	5.69897000433602	20308991	Integrative genome-wide association analysis of cytoarchitectural abnormalities in the prefrontal cortex of psychiatric disorders.	Brain cytoarchitecture	0	1	1	1
rs6658356	2E-6	5.69897000433602	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs17540621	2E-6	5.69897000433602	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs7979575	2E-6	5.69897000433602	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs314277	2E-6	5.69897000433602	20303062	A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure.	Digit length ratio	0	1	1	1
rs6584283	2E-6	5.69897000433602	20228798	Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL).	Ulcerative colitis	0	0	1	1
rs1032757	2E-6	5.69897000433602	20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Eosinophilic esophagitis (pediatric)	1	1	1	1
rs167769	2E-6	5.69897000433602	20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Eosinophilic esophagitis (pediatric)	0	1	1	1
rs2813746	2E-6	5.69897000433602	20197096	Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.	Brain structure (hippocampal volume)	1	1	1	1
rs1448284	2E-6	5.69897000433602	20197096	Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.	Brain structure (temporal lobe volume)	1	1	1	1
rs859637	2E-6	5.69897000433602	20190752	Multiple common variants for celiac disease influencing immune gene expression.	Celiac disease	NA	NA	NA	NA
rs7045881	2E-6	5.69897000433602	20185149	Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort.	Schizophrenia	1	1	1	1
rs17762192	2E-6	5.69897000433602	20064070	Multistage genomewide association study identifies a locus at 1q41 associated with rate of HIV-1 disease progression to clinical AIDS.	HIV-1 progression	0	1	1	1
rs6739054	2E-6	5.69897000433602	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs1343075	2E-6	5.69897000433602	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs9657451	2E-6	5.69897000433602	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	0	1	1	1
rs939876	2E-6	5.69897000433602	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs4775031	2E-6	5.69897000433602	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs882632	2E-6	5.69897000433602	20125088	Genome-wide association study of recurrent early-onset major depressive disorder.	Major depressive disorder	1	1	1	1
rs17525472	2E-6	5.69897000433602	20159242	Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions.	Asthma	1	1	1	1
rs10885122	2E-6	5.69897000433602	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	0	0	0
rs11248060	2E-6	5.69897000433602	20070850	Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.	Parkinson's disease	0	0	1	1
rs10499138	2E-6	5.69897000433602	20068591	A genome-wide association study for age-related hearing impairment in the Saami.	Hearing impairment	1	1	1	1
rs1036935	2E-6	5.69897000433602	20062064	Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk.	Chronic lymphocytic leukemia	1	1	1	1
rs1018326	2E-6	5.69897000433602	20062062	Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.	Ankylosing spondylitis	0	1	1	1
rs13053817	2E-6	5.69897000433602	20009918	A genome-wide association study of carotid atherosclerosis in HIV-infected men.	Carotid atherosclerosis in HIV infection	1	1	1	1
rs1697137	2E-6	5.69897000433602	20009918	A genome-wide association study of carotid atherosclerosis in HIV-infected men.	Carotid atherosclerosis in HIV infection	1	1	1	1
rs3763313	2E-6	5.69897000433602	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	0	1	1	1
rs4838508	2E-6	5.69897000433602	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs3734905	2E-6	5.69897000433602	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs4952590	2E-6	5.69897000433602	19961619	A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS).	Atopy	1	1	1	1
rs2833607	2E-6	5.69897000433602	19890347	Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8.	Vitiligo	1	1	1	1
rs7586898	2E-6	5.69897000433602	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	1	1	1	1
rs8057551	2E-6	5.69897000433602	19874204	IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study.	Bone mineral density	1	1	1	1
rs2383393	2E-6	5.69897000433602	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Body mass index	0	1	1	1
rs1522232	2E-6	5.69897000433602	19754311	Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03).	AIDS	1	1	1	1
rs9971637	2E-6	5.69897000433602	19734901	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs6592284	2E-6	5.69897000433602	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs7374394	2E-6	5.69897000433602	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs8043440	2E-6	5.69897000433602	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs2160519	2E-6	5.69897000433602	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs17001239	2E-6	5.69897000433602	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs6056209	2E-6	5.69897000433602	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs16832015	2E-6	5.69897000433602	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs1040994	2E-6	5.69897000433602	19721433	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics.	Response to antipsychotic treatment	1	1	1	1
rs7554607	2E-6	5.69897000433602	19684603	Germline genomic variants associated with childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs6881634	2E-6	5.69897000433602	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs4773460	2E-6	5.69897000433602	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs8115854	2E-6	5.69897000433602	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs2073145	2E-6	5.69897000433602	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs12476289	2E-6	5.69897000433602	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	QT interval	1	1	1	1
rs10488031	2E-6	5.69897000433602	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	QT interval	1	1	1	1
rs1533317	2E-6	5.69897000433602	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	QT interval	1	1	1	1
rs7601713	2E-6	5.69897000433602	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	QT interval	1	1	1	1
rs3743200	2E-6	5.69897000433602	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs4352210	2E-6	5.69897000433602	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs1484948	2E-6	5.69897000433602	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	0	1	1	1
rs2670321	2E-6	5.69897000433602	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs12552736	2E-6	5.69897000433602	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs4132509	2E-6	5.69897000433602	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs4701252	2E-6	5.69897000433602	19557197	NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium.	Waist circumference	1	1	1	1
rs6984045	2E-6	5.69897000433602	19525955	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.	Multiple sclerosis	1	1	1	1
rs6897932	2E-6	5.69897000433602	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs1250540	2E-6	5.69897000433602	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs4657482	2E-6	5.69897000433602	19483681	A genome-wide association study of testicular germ cell tumor.	Testicular germ cell tumor	0	0	1	1
rs11889862	2E-6	5.69897000433602	19448619	Loci at chromosomes 13, 19 and 20 influence age at natural menopause.	Menopause (age at onset)	1	1	1	1
rs2326679	2E-6	5.69897000433602	19448619	Loci at chromosomes 13, 19 and 20 influence age at natural menopause.	Menopause (age at onset)	1	1	1	1
rs1534422	2E-6	5.69897000433602	19430480	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs7250872	2E-6	5.69897000433602	19416921	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.	Bipolar disorder	1	1	1	1
rs1986655	2E-6	5.69897000433602	19414484	Genome-wide association meta-analysis for total serum bilirubin levels.	Bilirubin levels	1	1	1	1
rs4236644	2E-6	5.69897000433602	19414484	Genome-wide association meta-analysis for total serum bilirubin levels.	Bilirubin levels	1	1	1	1
rs7871764	2E-6	5.69897000433602	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	1	1	1	1
rs7969151	2E-6	5.69897000433602	19340012	Genome-wide association study of tanning phenotype in a population of European ancestry.	Tanning	1	1	1	1
rs526934	2E-6	5.69897000433602	19303062	Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations.	Folate pathway vitamin levels	0	0	1	1
rs642961	2E-6	5.69897000433602	19270707	Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.	Orofacial clefts	0	0	1	1
rs6693882	2E-6	5.69897000433602	19207018	Genome-wide association study of acute post-surgical pain in humans.	Pain	1	1	1	1
rs4787483	2E-6	5.69897000433602	19260139	Genome-wide association study of anthropometric traits in Korcula Island, Croatia.	Anthropometric traits	0	1	1	1
rs12207601	2E-6	5.69897000433602	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	1	1	1	1
rs4599440	2E-6	5.69897000433602	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	1	1	1	1
rs346923	2E-6	5.69897000433602	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	1	1	1	1
rs6125048	2E-6	5.69897000433602	19176441	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.	Response to treatment for acute lymphoblastic leukemia	1	1	1	1
rs7199343	2E-6	5.69897000433602	19132087	A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease.	Kawasaki disease	1	1	1	1
rs668853	2E-6	5.69897000433602	19122664	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.	Ulcerative colitis	1	1	1	1
rs2061333	2E-6	5.69897000433602	19118814	Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease.	Alzheimer's disease	0	1	1	1
rs972275	2E-6	5.69897000433602	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	1	1	1
rs2430212	2E-6	5.69897000433602	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	NA	NA	NA	NA
rs1867504	2E-6	5.69897000433602	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	0	0	0
rs10500991	2E-6	5.69897000433602	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	1	1	1	1
rs6735786	2E-6	5.69897000433602	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (hip)	1	1	1	1
rs2115172	2E-6	5.69897000433602	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	1	1	1
rs11719664	2E-6	5.69897000433602	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	1	1	1	1
rs6968385	2E-6	5.69897000433602	18937294	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.	Attention deficit hyperactivity disorder (time to onset)	1	1	1	1
rs6719977	2E-6	5.69897000433602	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Hyperactive-impulsive symptoms	1	1	1	1
rs7816032	2E-6	5.69897000433602	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Hyperactive-impulsive symptoms	0	1	1	1
rs12679254	2E-6	5.69897000433602	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	1	1	1	1
rs6832769	2E-6	5.69897000433602	18957941	Genome-wide association scan for five major dimensions of personality.	Personality dimensions	1	1	1	1
rs1458175	2E-6	5.69897000433602	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs1529316	2E-6	5.69897000433602	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs1386330	2E-6	5.69897000433602	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (age of onset)	1	1	1	1
rs12638253	2E-6	5.69897000433602	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (severity)	0	1	1	1
rs1478091	2E-6	5.69897000433602	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (severity)	1	1	1	1
rs12251307	2E-6	5.69897000433602	18978792	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.	Type 1 diabetes	0	0	1	1
rs11159647	2E-6	5.69897000433602	18976728	Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE.	Alzheimer's disease	1	1	1	1
rs10831284	2E-6	5.69897000433602	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs2826340	2E-6	5.69897000433602	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs1983853	2E-6	5.69897000433602	18840781	Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.	Type 1 diabetes	1	1	1	1
rs2199161	2E-6	5.69897000433602	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs2502731	2E-6	5.69897000433602	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs10786284	2E-6	5.69897000433602	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs1161463	2E-6	5.69897000433602	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Attention deficit hyperactivity disorder symptoms (interaction)	1	1	1	1
rs4714261	2E-6	5.69897000433602	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Attention deficit hyperactivity disorder symptoms (interaction)	1	1	1	1
rs13188771	2E-6	5.69897000433602	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	1	1	1	1
rs7595412	2E-6	5.69897000433602	18776929	Identification of PLCL1 gene for hip bone size variation in females in a genome-wide association study.	Hip bone size	1	1	1	1
rs4771450	2E-6	5.69897000433602	18759275	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish.	Uric acid levels	1	1	1	1
rs11150610	2E-6	5.69897000433602	19165918	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.	Systemic lupus erythematosus	0	0	1	1
rs854555	2E-6	5.69897000433602	18615156	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.	Response to TNF antagonist treatment	0	1	1	1
rs4541776	2E-6	5.69897000433602	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	NA	NA	NA	NA
rs710841	2E-6	5.69897000433602	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs2187642	2E-6	5.69897000433602	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs11611208	2E-6	5.69897000433602	18391951	Many sequence variants affecting diversity of adult human height.	Height	1	1	1	1
rs12449568	2E-6	5.69897000433602	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	1	1	1	1
rs7993214	2E-6	5.69897000433602	18369459	A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci.	Psoriasis	1	1	1	1
rs4939827	2E-6	5.69897000433602	18372905	A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.	Colorectal cancer	0	0	1	1
rs10486567	2E-6	5.69897000433602	18264096	Multiple loci identified in a genome-wide association study of prostate cancer.	Prostate cancer	1	1	1	1
rs1393350	2E-6	5.69897000433602	17952075	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Skin sensitivity to sun	0	1	0	0
rs1417352	2E-6	5.69897000433602	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	1	1	1	1
rs583012	2E-6	5.69897000433602	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	1	1	1	1
rs1486139	2E-6	5.69897000433602	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	1	1	1	1
rs10492681	2E-6	5.69897000433602	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	1	1	1	1
rs1106684	2E-6	5.69897000433602	17903300	Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.	Body mass index	0	0	0	0
rs1875517	2E-6	5.69897000433602	17903300	Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.	Waist circumference	1	1	1	1
rs1712790	2E-6	5.69897000433602	17903292	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.	Urinary albumin excretion	1	1	1	1
rs9291683	2E-6	5.69897000433602	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Bone mineral density	0	1	1	1
rs4131805	2E-6	5.69897000433602	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	1	1	1	1
rs922948	2E-6	5.69897000433602	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	1	1	1	1
rs10493340	2E-6	5.69897000433602	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Blood pressure	1	1	1	1
rs6063312	2E-6	5.69897000433602	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Tonometry	0	1	1	1
rs3793427	2E-6	5.69897000433602	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Tonometry	0	1	1	1
rs6492654	2E-6	5.69897000433602	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Tonometry	NA	NA	NA	NA
rs958672	2E-6	5.69897000433602	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Aging traits	1	1	1	1
rs2877832	2E-6	5.69897000433602	17903298	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	Diabetes related insulin traits	1	1	1	1
rs1926657	2E-6	5.69897000433602	17903305	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	Breast cancer	1	1	1	1
rs9311171	2E-6	5.69897000433602	17903305	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	Prostate cancer	1	1	1	1
rs1529276	2E-6	5.69897000433602	17903305	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	Prostate cancer	0	1	1	1
rs3849150	2E-6	5.69897000433602	17903303	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	Subclinical atherosclerosis traits (other)	1	1	1	1
rs1155865	2E-6	5.69897000433602	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Cognitive test performance	1	1	1	1
rs2832077	2E-6	5.69897000433602	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Cognitive test performance	1	1	1	1
rs2352904	2E-6	5.69897000433602	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Cognitive test performance	1	1	1	1
rs6914079	2E-6	5.69897000433602	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Cognitive test performance	0	1	1	1
rs366676	2E-6	5.69897000433602	17903301	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	Echocardiographic traits	1	1	1	1
rs441051	2E-6	5.69897000433602	17903307	Framingham Heart Study genome-wide association: results for pulmonary function measures.	Mean forced vital capacity from 2 exams	1	1	1	1
rs10493485	2E-6	5.69897000433602	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs7844723	2E-6	5.69897000433602	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs702543	2E-6	5.69897000433602	17667963	A whole genome association study of neuroticism using DNA pooling.	Neuroticism	1	1	1	1
rs17672135	2E-6	5.69897000433602	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Coronary heart disease	1	1	1	1
rs9469220	2E-6	5.69897000433602	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Crohn's disease	0	1	0	0
rs10761659	2E-6	5.69897000433602	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Crohn's disease	0	0	1	1
rs2837960	2E-6	5.69897000433602	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Rheumatoid arthritis	1	1	1	1
rs6534347	2E-6	5.69897000433602	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 1 diabetes	0	0	1	1
rs1801282	2E-6	5.69897000433602	17463246	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	Type 2 diabetes	0	0	1	1
rs1801282	2E-6	5.69897000433602	17463248	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.	Type 2 diabetes	0	0	1	1
rs1801282	2E-6	5.69897000433602	17463249	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs16984239	2E-6	5.69897000433602	17362836	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.	Amyotrophic lateral sclerosis	1	1	1	1
rs3858526	3E-6	5.52287874528034	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	1	1	1	1
rs17261688	3E-6	5.52287874528034	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	1	1	1	1
rs11640439	3E-6	5.52287874528034	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep duration	1	1	1	1
rs2042126	3E-6	5.52287874528034	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep duration	0	1	1	1
rs1005956	3E-6	5.52287874528034	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep quality	0	1	0	0
rs17071124	3E-6	5.52287874528034	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep quality	1	1	1	1
rs722258	3E-6	5.52287874528034	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep time	1	1	1	1
rs12582659	3E-6	5.52287874528034	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Cu levels)	1	1	1	1
rs3770549	3E-6	5.52287874528034	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Se levels)	1	1	1	1
rs679582	3E-6	5.52287874528034	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Se levels)	0	1	1	1
rs10812641	3E-6	5.52287874528034	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Se levels)	1	1	1	1
rs4333127	3E-6	5.52287874528034	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Zn levels)	1	1	1	1
rs10484100	3E-6	5.52287874528034	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Zn levels)	1	1	1	1
rs9958032	3E-6	5.52287874528034	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Zn levels)	1	1	1	1
rs4875284	3E-6	5.52287874528034	23698163	Genome-wide association study of serum selenium concentrations.	Serum selenium levels	NA	NA	NA	NA
rs8046148	3E-6	5.52287874528034	23666239	Meta-analysis identifies four new loci associated with testicular germ cell tumor.	Testicular germ cell tumor	0	0	1	1
rs4979078	3E-6	5.52287874528034	23650146	A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Venous thromboembolism	1	1	1	1
rs7164569	3E-6	5.52287874528034	23650146	A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Venous thromboembolism	0	1	1	1
rs2144300	3E-6	5.52287874528034	23620142	Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.	Circulating myeloperoxidase levels (serum) 	0	1	1	1
rs2045084	3E-6	5.52287874528034	23585552	Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.	Rhegmatogenous retinal detachment	1	1	1	1
rs2043090	3E-6	5.52287874528034	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	1	1	1	1
rs469339	3E-6	5.52287874528034	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	1	1	1	1
rs299362	3E-6	5.52287874528034	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs145379083	3E-6	5.52287874528034	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs8040855	3E-6	5.52287874528034	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs28631020	3E-6	5.52287874528034	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs1516459	3E-6	5.52287874528034	23568457	Genetic variants associated with disordered eating.	Eating disorders (purging via substances) 	1	1	1	1
rs6578985	3E-6	5.52287874528034	23593202	Bivariate genome-wide association analyses identified genes with pleiotropic effects for femoral neck bone geometry and age at menarche.	Femoral neck bone geometry and menarche (age at onset)	0	1	1	1
rs17530068	3E-6	5.52287874528034	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	0	0	1	1
rs2555603	3E-6	5.52287874528034	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (asthmatics)	1	1	1	1
rs13407913	3E-6	5.52287874528034	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (non-asthmatics)	0	0	0	0
rs1530016	3E-6	5.52287874528034	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (non-asthmatics)	0	0	0	0
rs1317830	3E-6	5.52287874528034	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (non-asthmatics)	0	1	1	1
rs4336372	3E-6	5.52287874528034	23555300	Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis.	Response to anti-TNF treatment in rheumatoid arthritis	0	0	0	0
rs4737547	3E-6	5.52287874528034	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs12659144	3E-6	5.52287874528034	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (hyperdiploidy)	1	1	1	1
rs10429371	3E-6	5.52287874528034	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Smooth-surface caries 	1	1	1	1
rs1268843	3E-6	5.52287874528034	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	0	1	1	1
rs10890920	3E-6	5.52287874528034	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	1	1	1	1
rs17450029	3E-6	5.52287874528034	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	0	1	1	1
rs786425	3E-6	5.52287874528034	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	1	1	1	1
rs10980926	3E-6	5.52287874528034	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	0	0	0
rs2609653	3E-6	5.52287874528034	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	0	0	0
rs2310173	3E-6	5.52287874528034	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs4730430	3E-6	5.52287874528034	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs11975235	3E-6	5.52287874528034	23509613	Genome-wide association study of antiphospholipid antibodies.	Presence of antiphospholipid antibodies	1	1	1	1
rs2357982	3E-6	5.52287874528034	23509613	Genome-wide association study of antiphospholipid antibodies.	Presence of antiphospholipid antibodies	0	1	1	1
rs9384488	3E-6	5.52287874528034	23419831	APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.	Alzheimer's disease biomarkers	1	1	1	1
rs17090640	3E-6	5.52287874528034	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs11624776	3E-6	5.52287874528034	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs7045138	3E-6	5.52287874528034	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	NA	NA	NA	NA
rs9378134	3E-6	5.52287874528034	23393555	Genome-wide association study of retinopathy in individuals without diabetes.	Retinopathy in non-diabetics	1	1	1	1
rs11826937	3E-6	5.52287874528034	23393555	Genome-wide association study of retinopathy in individuals without diabetes.	Retinopathy in non-diabetics	1	1	1	1
rs7930295	3E-6	5.52287874528034	23894747	A comprehensive family-based replication study of schizophrenia genes.	Schizophrenia	1	1	1	1
rs17634917	3E-6	5.52287874528034	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs2125000	3E-6	5.52287874528034	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs264272	3E-6	5.52287874528034	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs6598266	3E-6	5.52287874528034	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs2077147	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4745661	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2577704	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs3821819	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs13174348	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7361168	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs4869266	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7731390	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10108033	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs12451840	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10464366	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1531590	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11820502	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1467979	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6993449	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6466479	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs9886428	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11710456	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs17621444	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7108470	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6132333	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1823874	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs10995439	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs16906415	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs16982515	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1054052	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4710520	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11199254	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs12530	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11774682	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs3094093	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs10206020	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs16949825	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs16884711	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1952138	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6969802	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs12045693	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs3097645	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs12950390	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs2389339	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6059594	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7021663	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7215286	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11899928	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9468811	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6030171	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11188352	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6797769	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10813951	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10198756	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9636252	3E-6	5.52287874528034	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs12280105 	3E-6	5.52287874528034	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Oleic acid (18:1n-9) plasma levels	NA	NA	NA	NA
rs7561966 	3E-6	5.52287874528034	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitic acid (16:0) plasma levels	NA	NA	NA	NA
rs780093 	3E-6	5.52287874528034	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitic acid (16:0) plasma levels	NA	NA	NA	NA
rs12599426 	3E-6	5.52287874528034	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	NA	NA	NA	NA
rs7534537 	3E-6	5.52287874528034	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	NA	NA	NA	NA
rs2323397 	3E-6	5.52287874528034	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	NA	NA	NA	NA
rs12548021	3E-6	5.52287874528034	23350875	A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12.	Colorectal cancer	0	1	1	1
rs4530903	3E-6	5.52287874528034	23349640	Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.	Lymphoma	0	0	0	0
rs7092703	3E-6	5.52287874528034	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs1658442	3E-6	5.52287874528034	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	0	1	1	1
rs61970269	3E-6	5.52287874528034	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA)	1	1	1	1
rs11078884	3E-6	5.52287874528034	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA)	0	1	1	1
rs4680719	3E-6	5.52287874528034	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA)	1	1	1	1
rs2954793	3E-6	5.52287874528034	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA)	1	1	1	1
rs2836326	3E-6	5.52287874528034	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA)	1	1	1	1
rs1961649	3E-6	5.52287874528034	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/5-HIAA ratio)	1	1	1	1
rs181166265	3E-6	5.52287874528034	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs2482109	3E-6	5.52287874528034	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs742004	3E-6	5.52287874528034	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs6480975	3E-6	5.52287874528034	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	0	0	0
rs8020095	3E-6	5.52287874528034	23290196	A genome-wide association study of depressive symptoms.	Depression (quantitative trait)	1	1	1	1
rs6030	3E-6	5.52287874528034	23703922	A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls.	Uric acid levels	1	1	1	1
rs17730929	3E-6	5.52287874528034	23300701	Genome-wide search for gene-gene interactions in colorectal cancer.	Colorectal cancer	1	1	1	1
rs10114408	3E-6	5.52287874528034	23300701	Genome-wide search for gene-gene interactions in colorectal cancer.	Colorectal cancer	1	1	1	1
rs4591517	3E-6	5.52287874528034	23300701	Genome-wide search for gene-gene interactions in colorectal cancer.	Colorectal cancer	0	1	1	1
rs10879357	3E-6	5.52287874528034	23300701	Genome-wide search for gene-gene interactions in colorectal cancer.	Colorectal cancer	1	1	1	1
rs456867	3E-6	5.52287874528034	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs12468226	3E-6	5.52287874528034	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs2057314	3E-6	5.52287874528034	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	0	1	1	1
rs17094983	3E-6	5.52287874528034	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	1	1	1	1
rs9402592	3E-6	5.52287874528034	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs2046315	3E-6	5.52287874528034	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	0	1	1	1
rs10404998	3E-6	5.52287874528034	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	0	1	1	1
rs6011002	3E-6	5.52287874528034	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	0	1	1	1
rs12725198	3E-6	5.52287874528034	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	1	1	1	1
rs7324845	3E-6	5.52287874528034	23213074	Association between liver-specific gene polymorphisms and their expression levels with nonalcoholic fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs2383208	3E-6	5.52287874528034	23209189	Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21.	Type 2 diabetes	0	0	1	1
rs5758511	3E-6	5.52287874528034	23202124	New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.	Birth weight	0	1	1	1
rs2323266	3E-6	5.52287874528034	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	1	1	1	1
rs10900020	3E-6	5.52287874528034	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	1	1	1	1
rs11699237	3E-6	5.52287874528034	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	1	1	1	1
rs1455244	3E-6	5.52287874528034	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	1	1	1	1
rs10788473	3E-6	5.52287874528034	23180869	Genome-wide association study of survival in patients with pancreatic adenocarcinoma.	Pancreatic cancer	1	1	1	1
rs1000589	3E-6	5.52287874528034	23180869	Genome-wide association study of survival in patients with pancreatic adenocarcinoma.	Pancreatic cancer	1	1	1	1
rs903614	3E-6	5.52287874528034	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	1	1	1
rs12051723	3E-6	5.52287874528034	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity change in response to statin therapy	1	1	1	1
rs4596632	3E-6	5.52287874528034	23118974	Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations.	Eye color	0	1	1	1
rs3744728	3E-6	5.52287874528034	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	1	1	1	1
rs2860031	3E-6	5.52287874528034	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	1	1	1	1
rs7552806	3E-6	5.52287874528034	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs2476842	3E-6	5.52287874528034	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	0	1	1	1
rs2875517	3E-6	5.52287874528034	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs3788848	3E-6	5.52287874528034	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	NA	NA	NA	NA
rs931317	3E-6	5.52287874528034	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs13201929	3E-6	5.52287874528034	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs1045529	3E-6	5.52287874528034	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	0	0	0	0
rs656319	3E-6	5.52287874528034	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	0	1	1	1
rs7823896	3E-6	5.52287874528034	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs4792192	3E-6	5.52287874528034	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs2267138	3E-6	5.52287874528034	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs2280401	3E-6	5.52287874528034	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum total protein level	0	0	0	0
rs1364044	3E-6	5.52287874528034	22990015	A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke.	Stroke (pediatric)	1	1	1	1
rs10503672	3E-6	5.52287874528034	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis (age of onset)	1	1	1	1
rs472926	3E-6	5.52287874528034	22881374	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	Alzheimer's disease (late onset)	1	1	1	1
rs12210050	3E-6	5.52287874528034	22885689	Genome-wide association study of multiplex schizophrenia pedigrees.	Schizophrenia	0	1	1	1
rs9348876	3E-6	5.52287874528034	22936669	A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.	Crohn's disease	0	0	1	1
rs6894268	3E-6	5.52287874528034	22911880	Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits.	Eating disorders	1	1	1	1
rs7624327	3E-6	5.52287874528034	22911880	Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits.	Eating disorders	0	1	1	1
rs7414227	3E-6	5.52287874528034	22903471	Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.	Lentiform nucleus volume 	1	1	1	1
rs9499708	3E-6	5.52287874528034	22889921	Genome-wide association study of obsessive-compulsive disorder.	Obsessive-compulsive disorder	1	1	1	1
rs4703516	3E-6	5.52287874528034	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	NA	NA	NA	NA
rs7800244	3E-6	5.52287874528034	22841784	Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.	Hepatitis C induced liver fibrosis	1	1	1	1
rs3745367	3E-6	5.52287874528034	22843503	Genome-wide association analysis identifies TYW3/CRYZ and NDST4 loci associated with circulating resistin levels.	Resistin levels 	1	1	1	1
rs11209261	3E-6	5.52287874528034	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs2263638	3E-6	5.52287874528034	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs7607316	3E-6	5.52287874528034	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs1329705	3E-6	5.52287874528034	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	0	1	1	1
rs17065868	3E-6	5.52287874528034	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	1	1	1	1
rs1623523	3E-6	5.52287874528034	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	1	1	1	1
rs6719884	3E-6	5.52287874528034	23055271	Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.	Myasthenia gravis 	0	1	1	1
rs8064100	3E-6	5.52287874528034	22780124	Genome-wide association study of a quantitative disordered gambling trait.	Gambling	1	1	1	1
rs12237653	3E-6	5.52287874528034	22780124	Genome-wide association study of a quantitative disordered gambling trait.	Gambling	1	1	1	1
rs1247318	3E-6	5.52287874528034	22773346	Linkage and association of successful aging to the 6q25 region in large Amish kindreds.	Aging	1	1	1	1
rs7715172	3E-6	5.52287874528034	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	NA	NA	NA	NA
rs17135437	3E-6	5.52287874528034	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	NA	NA	NA	NA
rs2065779	3E-6	5.52287874528034	22754043	A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.	Insomnia (caffeine-induced)	0	1	1	1
rs16924631	3E-6	5.52287874528034	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	0	1	1	1
rs9523848	3E-6	5.52287874528034	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	0	1	1	1
rs2819348	3E-6	5.52287874528034	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs757978	3E-6	5.52287874528034	22700719	Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.	Chronic lymphocytic leukemia	0	0	1	1
rs821470	3E-6	5.52287874528034	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1484642	3E-6	5.52287874528034	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs3117099	3E-6	5.52287874528034	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs11653989	3E-6	5.52287874528034	22683750	A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern.	Cardiac repolarization	1	1	1	1
rs2727261	3E-6	5.52287874528034	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Estradiol levels	0	1	1	1
rs6721345	3E-6	5.52287874528034	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Sex hormone-binding globulin levels	NA	NA	NA	NA
rs11132733	3E-6	5.52287874528034	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Testosterone levels	NA	NA	NA	NA
rs11163372	3E-6	5.52287874528034	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	1	1	1	1
rs7387468	3E-6	5.52287874528034	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	1	1	1	1
rs10995356	3E-6	5.52287874528034	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	0	1	1	1
rs8004664	3E-6	5.52287874528034	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	1	1	1	1
rs2501677	3E-6	5.52287874528034	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	1	1	1	1
rs7903146	3E-6	5.52287874528034	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	0	1	0	0
rs1582861	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs2173063	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs2025934	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs12629805	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs1421084	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs227458	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs1502172	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	0	1	0	0
rs6781182	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs17216035	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs31872	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs8036080	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs10951138	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs6789987	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs4701523	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs6876835	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs7294372	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs13196329	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs13323436	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	0	1	1	1
rs815847	3E-6	5.52287874528034	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs7101446	3E-6	5.52287874528034	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs13073838	3E-6	5.52287874528034	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs2360111	3E-6	5.52287874528034	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs7984869	3E-6	5.52287874528034	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (fairness)	1	1	1	1
rs12434047	3E-6	5.52287874528034	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (fairness)	1	1	1	1
rs2120771	3E-6	5.52287874528034	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (feminism/equality)	1	1	1	1
rs4823246	3E-6	5.52287874528034	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (feminism/equality)	1	1	1	1
rs8090196	3E-6	5.52287874528034	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	0	0	0	0
rs11870477	3E-6	5.52287874528034	22569225	Investigation of single nucleotide polymorphisms and biological pathways associated with response to TNFα inhibitors in patients with rheumatoid arthritis.	Response to TNF-alpha inhibitors in rheumatoid arthritis	1	1	1	1
rs16992796	3E-6	5.52287874528034	22554406	Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6.	Electroencephalographic traits in alcoholism	1	1	1	1
rs7181753	3E-6	5.52287874528034	22554406	Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6.	Electroencephalographic traits in alcoholism	1	1	1	1
rs7328278	3E-6	5.52287874528034	22560479	Genome-wide association study of the age of onset of childhood asthma.	Asthma (childhood onset)	1	1	1	1
rs10521233	3E-6	5.52287874528034	22560479	Genome-wide association study of the age of onset of childhood asthma.	Asthma (childhood onset)	1	1	1	1
rs668459	3E-6	5.52287874528034	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	0	0	0
rs2785173	3E-6	5.52287874528034	22437554	Genome-wide association study identifies three common variants associated with serologic response to vitamin E supplementation in men.	Response to Vitamin E supplementation	1	1	1	1
rs2424234	3E-6	5.52287874528034	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs4822410	3E-6	5.52287874528034	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs10984561	3E-6	5.52287874528034	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs1906493	3E-6	5.52287874528034	22412388	A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.	Crohn's disease	1	1	1	1
rs12230440	3E-6	5.52287874528034	22379998	Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.	Adverse response to lamotrigine and phenytoin	1	1	1	1
rs9917256	3E-6	5.52287874528034	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	0	0	1	1
rs11026412	3E-6	5.52287874528034	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	1	1	1	1
rs4075511	3E-6	5.52287874528034	22365631	Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.	Temperament (bipolar disorder)	0	1	1	1
rs765787	3E-6	5.52287874528034	22229870	Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia.	Uric acid levels	1	1	1	1
rs488333	3E-6	5.52287874528034	22210626	Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.	Prion diseases	1	1	1	1
rs13130255	3E-6	5.52287874528034	22216198	A genome-wide association study of the Protein C anticoagulant pathway.	Anticoagulant levels	1	1	1	1
rs7335631	3E-6	5.52287874528034	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	1	1	1	1
rs1944766	3E-6	5.52287874528034	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	1	1	1	1
rs2254135	3E-6	5.52287874528034	22095909	Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.	Response to hepatitis C treatment	0	1	1	1
rs16864968	3E-6	5.52287874528034	22095909	Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.	Response to hepatitis C treatment	1	1	1	1
rs7156960	3E-6	5.52287874528034	22076464	Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	0	0	0	0
rs5968205	3E-6	5.52287874528034	22064162	Genome-wide association study of comorbid depressive syndrome and alcohol dependence.	Depression and alcohol dependence	NA	NA	NA	NA
rs17150687	3E-6	5.52287874528034	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	NA	NA	NA	NA
rs2163287	3E-6	5.52287874528034	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	NA	NA	NA	NA
rs10988449	3E-6	5.52287874528034	22041458	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	Response to antidepressant treatment	1	1	1	1
rs580140	3E-6	5.52287874528034	22044751	Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study.	Renal sinus fat 	1	1	1	1
rs6554809	3E-6	5.52287874528034	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	IgE grass sensitization	1	1	1	1
rs7617456	3E-6	5.52287874528034	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	IgE grass sensitization	1	1	1	1
rs271066	3E-6	5.52287874528034	22005931	Genome-wide association analysis of age-at-onset in Alzheimer's disease.	Alzheimer's disease (age of onset)	1	1	1	1
rs704454	3E-6	5.52287874528034	22005931	Genome-wide association analysis of age-at-onset in Alzheimer's disease.	Alzheimer's disease (age of onset)	1	1	1	1
rs17429217	3E-6	5.52287874528034	22005931	Genome-wide association analysis of age-at-onset in Alzheimer's disease.	Alzheimer's disease (age of onset)	1	1	1	1
rs2870137	3E-6	5.52287874528034	21993531	Genome-wide association study does not reveal major genetic determinants for anti-cytomegalovirus antibody response.	Cytomegalovirus antibody response	1	1	1	1
rs4084127	3E-6	5.52287874528034	21980299	A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.	Type 1 diabetes	1	1	1	1
rs1318937	3E-6	5.52287874528034	21956439	Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q.	Alcohol dependence	1	1	1	1
rs10894294	3E-6	5.52287874528034	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	0	1	1
rs1869901	3E-6	5.52287874528034	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	1	1	1	1
rs1009080	3E-6	5.52287874528034	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	1	1	1
rs2252865	3E-6	5.52287874528034	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	1	1	1
rs4660531	3E-6	5.52287874528034	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	1	1	1	1
rs7578035	3E-6	5.52287874528034	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	1	1	1	1
rs2287921	3E-6	5.52287874528034	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	0	1	1	1
rs12912251	3E-6	5.52287874528034	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	0	0	1	1
rs17398575	3E-6	5.52287874528034	21909108	Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.	Carotid intima media thickness	0	0	0	0
rs10235789	3E-6	5.52287874528034	21835309	GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development.	Iris characteristics	0	0	0	0
rs3761959	3E-6	5.52287874528034	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs4792814	3E-6	5.52287874528034	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs11755724	3E-6	5.52287874528034	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs793108	3E-6	5.52287874528034	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs10121009	3E-6	5.52287874528034	21812969	Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.	Parkinson's disease	1	1	1	1
rs7306642	3E-6	5.52287874528034	21810271	Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.	vWF and FVIII levels	1	1	1	1
rs10412199	3E-6	5.52287874528034	21782286	A genome-wide association study of aging.	Aging (time to event)	1	1	1	1
rs16852912	3E-6	5.52287874528034	21782286	A genome-wide association study of aging.	Aging (time to event)	1	1	1	1
rs8001976	3E-6	5.52287874528034	21782286	A genome-wide association study of aging.	Aging (time to event)	1	1	1	1
rs6122972	3E-6	5.52287874528034	21771265	Genome-wide association study on bipolar disorder in the Bulgarian population.	Bipolar disorder	1	1	1	1
rs2056626	3E-6	5.52287874528034	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	0	1	1
rs13021401	3E-6	5.52287874528034	21750679	Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.	Systemic sclerosis	1	1	1	1
rs2989476	3E-6	5.52287874528034	21738484	Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes.	Bipolar disorder	0	0	1	1
rs1014922	3E-6	5.52287874528034	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs12603284	3E-6	5.52287874528034	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs8028182	3E-6	5.52287874528034	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs1780436	3E-6	5.52287874528034	21621269	Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples.	Major depressive disorder	1	1	1	1
rs2154294	3E-6	5.52287874528034	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (12-month weekly alcohol consumption)	1	1	1	1
rs654128	3E-6	5.52287874528034	21460395	A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer.	Telomere length	0	1	1	1
rs2696835	3E-6	5.52287874528034	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs2115386	3E-6	5.52287874528034	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	0	1	1	1
rs7772697	3E-6	5.52287874528034	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs10199521	3E-6	5.52287874528034	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs1970671	3E-6	5.52287874528034	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs11265263	3E-6	5.52287874528034	21396408	Atopy history and the genomics of wheezing after influenza vaccination in children 6-59 months of age.	Vaccine-related adverse events 	0	1	1	1
rs3130320	3E-6	5.52287874528034	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	0	1	1	1
rs4027132	3E-6	5.52287874528034	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs7570682	3E-6	5.52287874528034	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs4520040	3E-6	5.52287874528034	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	1	1	1	1
rs769554	3E-6	5.52287874528034	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	NA	NA	NA	NA
rs2567426	3E-6	5.52287874528034	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs12915189	3E-6	5.52287874528034	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	0	1	1	1
rs793834	3E-6	5.52287874528034	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	0	1	1	1
rs11212364	3E-6	5.52287874528034	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs17124581	3E-6	5.52287874528034	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs1550976	3E-6	5.52287874528034	21182207	Variants in several genomic regions associated with asperger disorder.	Asperger disorder	1	1	1	1
rs6602175	3E-6	5.52287874528034	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	MRI atrophy measures	0	1	1	1
rs10510217	3E-6	5.52287874528034	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	0	1	1	1
rs4764039	3E-6	5.52287874528034	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	1	1	1	1
rs7153703	3E-6	5.52287874528034	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	1	1	1	1
rs3784609	3E-6	5.52287874528034	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	0	1	1	1
rs10512049	3E-6	5.52287874528034	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	1	1	1	1
rs6436839	3E-6	5.52287874528034	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Reasoning	1	1	1	1
rs4293296	3E-6	5.52287874528034	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Working memory	0	1	1	1
rs6707600	3E-6	5.52287874528034	21107309	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	Working memory	1	1	1	1
rs11007350	3E-6	5.52287874528034	21668797	A genome-wide association study of DSM-IV cannabis dependence.	Cannabis dependence	1	1	1	1
rs7617877	3E-6	5.52287874528034	21044948	Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.	Parkinson's disease	1	1	1	1
rs7319358	3E-6	5.52287874528034	20848476	Genetic predictors of medically refractory ulcerative colitis.	Ulcerative colitis	1	1	1	1
rs1488902	3E-6	5.52287874528034	20801717	Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.	Amyotrophic lateral sclerosis	1	1	1	1
rs11239177	3E-6	5.52287874528034	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs11072089	3E-6	5.52287874528034	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs11156606	3E-6	5.52287874528034	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	NA	NA	NA	NA
rs17111920	3E-6	5.52287874528034	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs2774292	3E-6	5.52287874528034	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs435746	3E-6	5.52287874528034	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs493187	3E-6	5.52287874528034	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs7386474	3E-6	5.52287874528034	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs358592	3E-6	5.52287874528034	20877300	Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project.	Suicidal ideation	1	1	1	1
rs4732812	3E-6	5.52287874528034	20877300	Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project.	Suicidal ideation	1	1	1	1
rs9943753	3E-6	5.52287874528034	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	HDL cholesterol	0	0	1	1
rs6867983	3E-6	5.52287874528034	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	Triglycerides	0	0	1	1
rs7121446	3E-6	5.52287874528034	20838585	Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.	Cardiovascular disease risk factors	1	1	1	1
rs12420464	3E-6	5.52287874528034	20800221	Genome-wide association scan of trait depression.	Depression (quantitative trait)	1	1	1	1
rs7326068	3E-6	5.52287874528034	20713499	Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression.	Schizophrenia, bipolar disorder and depression (combined)	1	1	1	1
rs3758354	3E-6	5.52287874528034	20713499	Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression.	Schizophrenia, bipolar disorder and depression (combined)	1	1	1	1
rs682238	3E-6	5.52287874528034	20705733	Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.	Calcium levels	0	1	1	1
rs2645424	3E-6	5.52287874528034	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (lobular)	0	1	0	0
rs2986971	3E-6	5.52287874528034	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (lobular)	1	1	1	1
rs1836127	3E-6	5.52287874528034	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs2800	3E-6	5.52287874528034	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs894177	3E-6	5.52287874528034	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs6798928	3E-6	5.52287874528034	20694011	Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.	Immunoglobulin A 	1	1	1	1
rs6573416	3E-6	5.52287874528034	20707712	A genome-wide association study of self-rated health.	Self-rated health	1	1	1	1
rs7463256	3E-6	5.52287874528034	20732625	Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	1	1	1	1
rs9943849	3E-6	5.52287874528034	20673876	Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression.	Major depressive disorder	1	1	1	1
rs7142002	3E-6	5.52287874528034	20663923	A genome-wide scan for common alleles affecting risk for autism.	Autism	1	1	1	1
rs2403106	3E-6	5.52287874528034	20662065	Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus.	Neonatal lupus	1	1	1	1
rs714052	3E-6	5.52287874528034	20657596	Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.	Hypertriglyceridemia	0	1	1	1
rs2241880	3E-6	5.52287874528034	20570966	Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.	Crohn's disease	0	0	1	1
rs2172802	3E-6	5.52287874528034	20522523	Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.	Partial epilepsies	1	1	1	1
rs606149	3E-6	5.52287874528034	20516156	Genome-wide association study of major recurrent depression in the U.K. population.	Major depressive disorder	1	1	1	1
rs3757318	3E-6	5.52287874528034	20453838	Genome-wide association study identifies five new breast cancer susceptibility loci.	Breast cancer	0	0	1	1
rs11782819	3E-6	5.52287874528034	20452100	Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study.	Alzheimer's disease	1	1	1	1
rs6473383	3E-6	5.52287874528034	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	1	1	1	1
rs13418717	3E-6	5.52287874528034	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	1	1	1	1
rs563519	3E-6	5.52287874528034	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	1	1	1	1
rs2046383	3E-6	5.52287874528034	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	0	1	1	1
rs2736428	3E-6	5.52287874528034	20421499	Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology.	Telomere length	0	1	1	1
rs12733856	3E-6	5.52287874528034	20400778	Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.	Mortality among heart failure patients	1	1	1	1
rs13095226	3E-6	5.52287874528034	20385826	Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).	Age-related macular degeneration	0	0	1	1
rs1126757	3E-6	5.52287874528034	20360315	Genome-wide pharmacogenetics of antidepressant response in the GENDEP project.	Response to antidepressants	1	1	1	1
rs4651156	3E-6	5.52287874528034	20360315	Genome-wide pharmacogenetics of antidepressant response in the GENDEP project.	Response to antidepressants	1	1	1	1
rs11666579	3E-6	5.52287874528034	20360315	Genome-wide pharmacogenetics of antidepressant response in the GENDEP project.	Response to antidepressants	1	1	1	1
rs4972755	3E-6	5.52287874528034	20351715	Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.	Bipolar disorder and major depressive disorder (combined)	1	1	1	1
rs13148903	3E-6	5.52287874528034	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs174583	3E-6	5.52287874528034	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	0	1	1	1
rs4781011	3E-6	5.52287874528034	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	1	1	1	1
rs1939875	3E-6	5.52287874528034	20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Eosinophilic esophagitis (pediatric)	1	1	1	1
rs2290720	3E-6	5.52287874528034	20197096	Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.	Brain structure (hippocampal volume)	1	1	1	1
rs11055612	3E-6	5.52287874528034	20197096	Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.	Brain structure (temporal lobe volume)	1	1	1	1
rs2817937	3E-6	5.52287874528034	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (number of teeth)	0	1	1	1
rs433598	3E-6	5.52287874528034	20185149	Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort.	Schizophrenia	1	1	1	1
rs7555668	3E-6	5.52287874528034	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs4397449	3E-6	5.52287874528034	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	NA	NA	NA	NA
rs1463984	3E-6	5.52287874528034	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs2807580	3E-6	5.52287874528034	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs17070284	3E-6	5.52287874528034	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	0	1	1	1
rs6496074	3E-6	5.52287874528034	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs3784962	3E-6	5.52287874528034	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	0	1	1	1
rs4145170	3E-6	5.52287874528034	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs10464059	3E-6	5.52287874528034	20070850	Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.	Parkinson's disease	1	1	1	1
rs10265216	3E-6	5.52287874528034	20038947	Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.	Major depressive disorder (broad)	1	1	1	1
rs11818629	3E-6	5.52287874528034	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs12198173	3E-6	5.52287874528034	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	0	0	0	0
rs12431733	3E-6	5.52287874528034	19915575	Genome-wide association study reveals genetic risk underlying Parkinson's disease.	Parkinson's disease	1	1	1	1
rs10503019	3E-6	5.52287874528034	19890347	Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8.	Vitiligo	1	1	1	1
rs261360	3E-6	5.52287874528034	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	1	1	1	1
rs12623288	3E-6	5.52287874528034	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	0	1	1	1
rs824931	3E-6	5.52287874528034	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Body mass index	1	1	1	1
rs1152846	3E-6	5.52287874528034	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Body mass index	0	1	1	1
rs7209395	3E-6	5.52287874528034	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Weight	0	1	1	1
rs17565841	3E-6	5.52287874528034	19772629	Genomewide association study for onset age in Parkinson disease.	Parkinson's disease (age of onset)	1	1	1	1
rs1360517	3E-6	5.52287874528034	19754311	Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03).	AIDS	1	1	1	1
rs774359	3E-6	5.52287874528034	19734901	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	0	0	0	0
rs2405657	3E-6	5.52287874528034	19734901	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs5916687	3E-6	5.52287874528034	19734901	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	NA	NA	NA	NA
rs4082514	3E-6	5.52287874528034	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	0	1	1	1
rs9036	3E-6	5.52287874528034	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs10279573	3E-6	5.52287874528034	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs12526186	3E-6	5.52287874528034	19721433	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics.	Response to antipsychotic treatment	0	1	1	1
rs17815774	3E-6	5.52287874528034	19721433	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics.	Response to antipsychotic treatment	1	1	1	1
rs7635839	3E-6	5.52287874528034	19721433	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics.	Response to antipsychotic treatment	1	1	1	1
rs12621643	3E-6	5.52287874528034	19684603	Germline genomic variants associated with childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs12476047	3E-6	5.52287874528034	19680635	Genome-wide association study of antipsychotic-induced parkinsonism severity among schizophrenia patients.	Response to antipsychotic treatment	1	1	1	1
rs10276619	3E-6	5.52287874528034	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	0	1	1	1
rs11525066	3E-6	5.52287874528034	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs10867752	3E-6	5.52287874528034	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs1530057	3E-6	5.52287874528034	19654303	Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.	Lung cancer	1	1	1	1
rs17706439	3E-6	5.52287874528034	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs893817	3E-6	5.52287874528034	19584346	Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.	Aortic root size	0	1	1	1
rs2059238	3E-6	5.52287874528034	19584346	Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.	Cardiac structure and function	0	1	1	1
rs10898392	3E-6	5.52287874528034	19570815	A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.	Height	1	1	1	1
rs1864982	3E-6	5.52287874528034	19581569	Genome-wide association study of alcohol dependence.	Alcohol dependence	0	1	1	1
rs1555967	3E-6	5.52287874528034	19557197	NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium.	Waist circumference	1	1	1	1
rs10433903	3E-6	5.52287874528034	19553259	Common body mass index-associated variants confer risk of extreme obesity.	Obesity (extreme)	1	1	1	1
rs6604026	3E-6	5.52287874528034	19525955	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.	Multiple sclerosis	0	0	1	1
rs10038113	3E-6	5.52287874528034	19456320	A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.	Autism	0	0	1	1
rs10499859	3E-6	5.52287874528034	19454037	Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study.	Left ventricular mass	1	1	1	1
rs11241713	3E-6	5.52287874528034	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs4906172	3E-6	5.52287874528034	19448619	Loci at chromosomes 13, 19 and 20 influence age at natural menopause.	Menopause (age at onset)	0	1	1	1
rs13409348	3E-6	5.52287874528034	19416921	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.	Bipolar disorder	1	1	1	1
rs6733011	3E-6	5.52287874528034	19416921	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.	Bipolar disorder	0	0	1	1
rs2162440	3E-6	5.52287874528034	19359265	A genome-wide association study identifies a novel locus on chromosome 18q12.2 influencing white cell telomere length.	Telomere length	1	1	1	1
rs7279297	3E-6	5.52287874528034	19340012	Genome-wide association study of tanning phenotype in a population of European ancestry.	Tanning	1	1	1	1
rs910696	3E-6	5.52287874528034	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	0	1	1	1
rs7553864	3E-6	5.52287874528034	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	1	1	1	1
rs800082	3E-6	5.52287874528034	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	1	1	1	1
rs2269426	3E-6	5.52287874528034	19198610	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.	Eosinophil counts	0	1	1	1
rs7157940	3E-6	5.52287874528034	19260139	Genome-wide association study of anthropometric traits in Korcula Island, Croatia.	Anthropometric traits	1	1	1	1
rs1490453	3E-6	5.52287874528034	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	1	1	1	1
rs7885458	3E-6	5.52287874528034	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	NA	NA	NA	NA
rs871392	3E-6	5.52287874528034	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	1	1	1	1
rs4723619	3E-6	5.52287874528034	19176441	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.	Response to treatment for acute lymphoblastic leukemia	1	1	1	1
rs6971925	3E-6	5.52287874528034	19176441	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.	Response to treatment for acute lymphoblastic leukemia	1	1	1	1
rs973968	3E-6	5.52287874528034	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	1	1	1	1
rs1457451	3E-6	5.52287874528034	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	1	1	1	1
rs7481311	3E-6	5.52287874528034	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Weight	0	0	0	0
rs6987702	3E-6	5.52287874528034	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	LDL cholesterol	0	0	0	0
rs2304130	3E-6	5.52287874528034	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	LDL cholesterol	0	0	0	0
rs2304130	3E-6	5.52287874528034	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	Triglycerides	0	0	0	0
rs1514928	3E-6	5.52287874528034	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	1	1	1	1
rs7577925	3E-6	5.52287874528034	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	0	1	1	1
rs11590090	3E-6	5.52287874528034	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Hyperactive-impulsive symptoms	1	1	1	1
rs10895959	3E-6	5.52287874528034	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	1	1	1	1
rs7495052	3E-6	5.52287874528034	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	1	1	1	1
rs17281813	3E-6	5.52287874528034	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	NA	NA	NA	NA
rs2769967	3E-6	5.52287874528034	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	1	1	1	1
rs2540226	3E-6	5.52287874528034	18957941	Genome-wide association scan for five major dimensions of personality.	Personality dimensions	1	1	1	1
rs908821	3E-6	5.52287874528034	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs1755289	3E-6	5.52287874528034	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs17157903	3E-6	5.52287874528034	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (age of onset)	1	1	1	1
rs2116078	3E-6	5.52287874528034	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (age of onset)	1	1	1	1
rs10260404	3E-6	5.52287874528034	18987618	Screening for replication of genome-wide SNP associations in sporadic ALS.	Amyotrophic lateral sclerosis	0	0	1	1
rs416603	3E-6	5.52287874528034	18978792	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.	Type 1 diabetes	0	1	1	1
rs10758593	3E-6	5.52287874528034	18840781	Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.	Type 1 diabetes	0	0	1	1
rs2842643	3E-6	5.52287874528034	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs6500744	3E-6	5.52287874528034	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	1	1	1	1
rs1789891	3E-6	5.52287874528034	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	0	1	1	1
rs727153	3E-6	5.52287874528034	18823527	A genome-wide association study for late-onset Alzheimer's disease using DNA pooling.	Alzheimer's disease	1	1	1	1
rs4668338	3E-6	5.52287874528034	18759275	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish.	Uric acid levels	0	1	1	1
rs2314398	3E-6	5.52287874528034	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	0	0	1	1
rs4130590	3E-6	5.52287874528034	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	1	1	1	1
rs11101442	3E-6	5.52287874528034	19165918	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.	Systemic lupus erythematosus	0	1	1	1
rs1602565	3E-6	5.52287874528034	18677311	Identification of loci associated with schizophrenia by genome-wide association and follow-up.	Schizophrenia	1	1	1	1
rs6138150	3E-6	5.52287874528034	18615156	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.	Response to TNF antagonist treatment	1	1	1	1
rs10874639	3E-6	5.52287874528034	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs2081670	3E-6	5.52287874528034	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs1779876	3E-6	5.52287874528034	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs11637235	3E-6	5.52287874528034	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs2729409	3E-6	5.52287874528034	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs4140564	3E-6	5.52287874528034	18471798	Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis.	Knee osteoarthritis	1	1	1	1
rs11177669	3E-6	5.52287874528034	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs1474563	3E-6	5.52287874528034	18391951	Many sequence variants affecting diversity of adult human height.	Height	NA	NA	NA	NA
rs11243676	3E-6	5.52287874528034	18204098	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.	Systemic lupus erythematosus	1	1	1	1
rs10078095	3E-6	5.52287874528034	18193045	Common variants in the GDF5-UQCC region are associated with variation in human height.	Height	1	1	1	1
rs10260404	3E-6	5.52287874528034	18057069	A genome-wide association study of sporadic ALS in a homogenous Irish population.	Amyotrophic lateral sclerosis	0	0	1	1
rs10507577	3E-6	5.52287874528034	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	1	1	1	1
rs1079596	3E-6	5.52287874528034	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	1	1	1	1
rs1474747	3E-6	5.52287874528034	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	0	0	0	0
rs7778619	3E-6	5.52287874528034	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	1	1	1	1
rs2218488	3E-6	5.52287874528034	17903308	Genome-wide association of sleep and circadian phenotypes.	Sleepiness	1	1	1	1
rs10510628	3E-6	5.52287874528034	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Bone mineral density	1	1	1	1
rs2214681	3E-6	5.52287874528034	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Bone mineral density	1	1	1	1
rs4715166	3E-6	5.52287874528034	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	1	1	1	1
rs1590305	3E-6	5.52287874528034	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	1	1	1	1
rs10492096	3E-6	5.52287874528034	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	1	1	1	1
rs1963982	3E-6	5.52287874528034	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Blood pressure	1	1	1	1
rs935334	3E-6	5.52287874528034	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Blood pressure	1	1	1	1
rs770189	3E-6	5.52287874528034	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Tonometry	0	1	1	1
rs1367248	3E-6	5.52287874528034	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Tonometry	1	1	1	1
rs2371208	3E-6	5.52287874528034	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Aging traits	1	1	1	1
rs2877832	3E-6	5.52287874528034	17903298	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	Diabetes related insulin traits	0	0	0	0
rs10263639	3E-6	5.52287874528034	17903305	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	Breast cancer	1	1	1	1
rs10498792	3E-6	5.52287874528034	17903305	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	Prostate cancer	0	1	1	1
rs4466137	3E-6	5.52287874528034	17903305	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	Prostate cancer	1	1	1	1
rs9325032	3E-6	5.52287874528034	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Cognitive test performance	0	1	1	1
rs3891355	3E-6	5.52287874528034	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Cognitive test performance	0	1	1	1
rs2847476	3E-6	5.52287874528034	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Volumetric brain MRI	1	1	1	1
rs5028798	3E-6	5.52287874528034	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Volumetric brain MRI	1	1	1	1
rs6847149	3E-6	5.52287874528034	17903301	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	Exercise treadmill test traits	1	1	1	1
rs2838815	3E-6	5.52287874528034	17903307	Framingham Heart Study genome-wide association: results for pulmonary function measures.	Pulmonary function	1	1	1	1
rs4460176	3E-6	5.52287874528034	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs2306677	3E-6	5.52287874528034	17827064	ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study.	Amyotrophic lateral sclerosis	1	1	1	1
rs1793004	3E-6	5.52287874528034	17684544	Systematic association mapping identifies NELL1 as a novel IBD disease gene.	Crohn's disease	1	1	1	1
rs6596075	3E-6	5.52287874528034	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Crohn's disease	0	0	1	1
rs17388568	3E-6	5.52287874528034	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 1 diabetes	0	0	0	0
rs358806	3E-6	5.52287874528034	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 2 diabetes	1	1	1	1
rs1800775	3E-6	5.52287874528034	17463246	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	Triglycerides	0	0	0	0
rs13266634	3E-6	5.52287874528034	17460697	A variant in CDKAL1 influences insulin response and risk of type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs12680546	3E-6	5.52287874528034	17362836	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.	Amyotrophic lateral sclerosis	1	1	1	1
rs1111875	3E-6	5.52287874528034	17293876	A genome-wide association study identifies novel risk loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs7644516	4E-6	5.39794000867204	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	1	1	1	1
rs11987678	4E-6	5.39794000867204	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep duration	1	1	1	1
rs2302729	4E-6	5.39794000867204	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep quality	1	1	1	1
rs1478693	4E-6	5.39794000867204	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep time	1	1	1	1
rs1539808	4E-6	5.39794000867204	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep time	1	1	1	1
rs3857536	4E-6	5.39794000867204	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Cu levels)	1	1	1	1
rs7129556	4E-6	5.39794000867204	23643386	Weight loss after gastric bypass is associated with a variant at 15q26.1.	Weight loss (gastric bypass surgery)	1	1	1	1
rs7185923	4E-6	5.39794000867204	23643386	Weight loss after gastric bypass is associated with a variant at 15q26.1.	Weight loss (gastric bypass surgery)	1	1	1	1
rs10213084	4E-6	5.39794000867204	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	1	1	1	1
rs114945094	4E-6	5.39794000867204	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	1	1	1	1
rs77742018	4E-6	5.39794000867204	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	1	1	1	1
rs1937020	4E-6	5.39794000867204	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	0	1	1	1
rs12986207	4E-6	5.39794000867204	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs115694618	4E-6	5.39794000867204	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	0	1	1	1
rs10906233	4E-6	5.39794000867204	23568457	Genetic variants associated with disordered eating.	Eating disorders	1	1	1	1
rs11087123	4E-6	5.39794000867204	23568457	Genetic variants associated with disordered eating.	Eating disorders	1	1	1	1
rs138206701	4E-6	5.39794000867204	23568457	Genetic variants associated with disordered eating.	Eating disorders	0	1	0	0
rs10998035	4E-6	5.39794000867204	23568457	Genetic variants associated with disordered eating.	Eating disorders (purging via substances) 	0	1	1	1
rs1631486	4E-6	5.39794000867204	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	0	1	1	1
rs713587	4E-6	5.39794000867204	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (non-asthmatics)	0	0	0	0
rs765855	4E-6	5.39794000867204	23544013	Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.	Breast Cancer in BRCA1 mutation carriers	1	1	1	1
rs1291183	4E-6	5.39794000867204	23541324	Genome-wide association study identifies TH1 pathway genes associated with lung function in asthmatic patients.	Pulmonary function in asthmatics	1	1	1	1
rs7536700	4E-6	5.39794000867204	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs3096299	4E-6	5.39794000867204	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	0	0	0	0
rs2032381	4E-6	5.39794000867204	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Smooth-surface caries 	1	1	1	1
rs230014	4E-6	5.39794000867204	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	1	1	1	1
rs3217869	4E-6	5.39794000867204	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	0	1	1	1
rs2708240	4E-6	5.39794000867204	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	1	1	1	1
rs7953508	4E-6	5.39794000867204	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs7751505	4E-6	5.39794000867204	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs10873998	4E-6	5.39794000867204	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs7700191	4E-6	5.39794000867204	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs2186903	4E-6	5.39794000867204	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs447	4E-6	5.39794000867204	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs10219670	4E-6	5.39794000867204	23419831	APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.	Alzheimer's disease biomarkers	1	1	1	1
rs5978649	4E-6	5.39794000867204	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	NA	NA	NA	NA
rs7553035	4E-6	5.39794000867204	23393555	Genome-wide association study of retinopathy in individuals without diabetes.	Retinopathy in non-diabetics	1	1	1	1
rs6472155	4E-6	5.39794000867204	23393555	Genome-wide association study of retinopathy in individuals without diabetes.	Retinopathy in non-diabetics	1	1	1	1
rs17194885	4E-6	5.39794000867204	23393555	Genome-wide association study of retinopathy in individuals without diabetes.	Retinopathy in non-diabetics	1	1	1	1
rs6917824L	4E-6	5.39794000867204	23894747	A comprehensive family-based replication study of schizophrenia genes.	Schizophrenia	NA	NA	NA	NA
rs1046089	4E-6	5.39794000867204	23894747	A comprehensive family-based replication study of schizophrenia genes.	Schizophrenia	0	1	1	1
rs264272	4E-6	5.39794000867204	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	0	0	0	0
rs17710780	4E-6	5.39794000867204	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs9466930	4E-6	5.39794000867204	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs364477	4E-6	5.39794000867204	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs8012941	4E-6	5.39794000867204	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs1673101	4E-6	5.39794000867204	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs4711279	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs16844841	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2900	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1439523	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4866334	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs444881	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs9296009	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs322668	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9308433	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10937705	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10834691	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2219937	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs13323323	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2361701	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10206020	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1319535	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs17835853	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs12750249	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10488029	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs7314811	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6547537	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11745890	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11765886	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6928844	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2745851	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs592229	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2186369	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs3813009	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10203166	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1547201	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2302105	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7179432	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9563960	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1953652	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6466479	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1058065	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs13272623	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs523516	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2844479	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs1577330	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs16844846	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs9490860	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs435066	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11581667	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2610739	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs3777193	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7397814	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2292298	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6059594	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11635553	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs16944158	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7582701	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs12127944	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs17348299	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2080501	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1012583	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2280655	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs627386	4E-6	5.39794000867204	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10234749 	4E-6	5.39794000867204	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitic acid (16:0) plasma levels	NA	NA	NA	NA
rs1980946 	4E-6	5.39794000867204	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitic acid (16:0) plasma levels	NA	NA	NA	NA
rs16949516 	4E-6	5.39794000867204	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Stearic acid (18:0) plasma levels	NA	NA	NA	NA
rs4555772 	4E-6	5.39794000867204	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Stearic acid (18:0) plasma levels	NA	NA	NA	NA
rs3104964	4E-6	5.39794000867204	23350875	A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12.	Colorectal cancer	1	1	1	1
rs77265424	4E-6	5.39794000867204	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA)	NA	NA	NA	NA
rs13207034	4E-6	5.39794000867204	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA)	0	1	0	0
rs68184094	4E-6	5.39794000867204	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA-5-HIAA Factor score)	0	1	0	0
rs187200046	4E-6	5.39794000867204	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA-5-HIAA Factor score)	0	1	0	0
rs78546022	4E-6	5.39794000867204	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/5-HIAA ratio)	1	1	1	1
rs11031492	4E-6	5.39794000867204	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/5-HIAA ratio)	1	1	1	1
rs3795958	4E-6	5.39794000867204	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	0	1	0	0
rs6750634	4E-6	5.39794000867204	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs6526555	4E-6	5.39794000867204	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	NA	NA	NA	NA
rs11689435	4E-6	5.39794000867204	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	0	1	1	1
rs3884558	4E-6	5.39794000867204	23319801	Identification of inherited genetic variations influencing prognosis in early-onset breast cancer.	Breast cancer (prognosis)	1	1	1	1
rs1387389	4E-6	5.39794000867204	23319801	Identification of inherited genetic variations influencing prognosis in early-onset breast cancer.	Breast cancer (prognosis)	1	1	1	1
rs621313	4E-6	5.39794000867204	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	1	1	1
rs9365723	4E-6	5.39794000867204	23300701	Genome-wide search for gene-gene interactions in colorectal cancer.	Colorectal cancer	1	1	1	1
rs11954519	4E-6	5.39794000867204	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs9793739	4E-6	5.39794000867204	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	0	0	0	0
rs2888830	4E-6	5.39794000867204	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs4269515	4E-6	5.39794000867204	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs1344555	4E-6	5.39794000867204	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs2341260	4E-6	5.39794000867204	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	1	1	1	1
rs6983473	4E-6	5.39794000867204	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	1	1	1	1
rs13083990	4E-6	5.39794000867204	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	0	1	1	1
rs10461617	4E-6	5.39794000867204	23209189	Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21.	Type 2 diabetes	0	1	1	1
rs11165354	4E-6	5.39794000867204	23209189	Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21.	Type 2 diabetes	1	1	1	1
rs10052004	4E-6	5.39794000867204	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	1	1	1	1
rs7172342	4E-6	5.39794000867204	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	1	1	1	1
rs4798896	4E-6	5.39794000867204	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	1	1	1	1
rs9874556	4E-6	5.39794000867204	23180869	Genome-wide association study of survival in patients with pancreatic adenocarcinoma.	Pancreatic cancer	1	1	1	1
rs954820	4E-6	5.39794000867204	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	1	1	1	1
rs3751143	4E-6	5.39794000867204	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	1	1	1	1
rs10782529	4E-6	5.39794000867204	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity change in response to statin therapy	1	1	1	1
rs3934861	4E-6	5.39794000867204	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	1	1	1	1
rs11704416	4E-6	5.39794000867204	23065704	A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease.	Prostate cancer	0	0	0	0
rs357894	4E-6	5.39794000867204	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	0	1	1	1
rs2864527	4E-6	5.39794000867204	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs735539	4E-6	5.39794000867204	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	0	1	1	1
rs2441755	4E-6	5.39794000867204	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs13381277	4E-6	5.39794000867204	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs11723530	4E-6	5.39794000867204	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs804280	4E-6	5.39794000867204	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	0	1	1	1
rs12803066	4E-6	5.39794000867204	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs2107595	4E-6	5.39794000867204	23041239	Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.	Stroke (ischemic)	0	0	0	0
rs1260326	4E-6	5.39794000867204	23022100	Discovery and fine mapping of serum protein loci through transethnic meta-analysis.	Serum total protein level	0	0	0	0
rs10170236	4E-6	5.39794000867204	23007406	Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs2084898	4E-6	5.39794000867204	22990015	A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke.	Stroke (pediatric)	0	0	0	0
rs10998466	4E-6	5.39794000867204	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs1981483	4E-6	5.39794000867204	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	1	1	1
rs1154053	4E-6	5.39794000867204	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs2484990	4E-6	5.39794000867204	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs1250307	4E-6	5.39794000867204	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs7204439	4E-6	5.39794000867204	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs7146198	4E-6	5.39794000867204	22969067	Genetic variants near PDGFRA are associated with corneal curvature in Australians.	Corneal curvature	1	1	1	1
rs9533799	4E-6	5.39794000867204	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	1	1	1	1
rs11890028	4E-6	5.39794000867204	22949513	Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32	Epilepsy (generalized)	1	1	1	1
rs12426725	4E-6	5.39794000867204	22885689	Genome-wide association study of multiplex schizophrenia pedigrees.	Schizophrenia	1	1	1	1
rs12210050	4E-6	5.39794000867204	22885689	Genome-wide association study of multiplex schizophrenia pedigrees.	Schizophrenia	0	0	0	0
rs4077515	4E-6	5.39794000867204	22936669	A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.	Crohn's disease	0	0	1	1
rs11264736	4E-6	5.39794000867204	22903471	Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.	Lentiform nucleus volume 	0	0	0	0
rs10496584	4E-6	5.39794000867204	22903471	Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.	Lentiform nucleus volume 	1	1	1	1
rs9975851	4E-6	5.39794000867204	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs1573535	4E-6	5.39794000867204	22823124	The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation.	Cannabis use (initiation)	1	1	1	1
rs185694	4E-6	5.39794000867204	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	1	1	1	1
rs11060736	4E-6	5.39794000867204	22780124	Genome-wide association study of a quantitative disordered gambling trait.	Gambling	1	1	1	1
rs4398173	4E-6	5.39794000867204	22760553	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Response to citalopram treatment	0	0	0	0
rs8044769	4E-6	5.39794000867204	22763110	Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study.	Osteoarthritis	0	1	1	1
rs11706236	4E-6	5.39794000867204	22754043	A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.	Insomnia (caffeine-induced)	1	1	1	1
rs2388082	4E-6	5.39794000867204	22754043	A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.	Insomnia (caffeine-induced)	1	1	1	1
rs10010758	4E-6	5.39794000867204	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	1	1	1	1
rs1970525	4E-6	5.39794000867204	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	1	1	1	1
rs11800854	4E-6	5.39794000867204	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	0	0	0	0
rs9287989	4E-6	5.39794000867204	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	1	1	1	1
rs580384	4E-6	5.39794000867204	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs11680012	4E-6	5.39794000867204	22739583	A Variant in the LRRFIP1 Gene Is Associated With Adiposity and Inflammation.	Adiposity	1	1	1	1
rs10033900	4E-6	5.39794000867204	22705344	Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.	Age-related macular degeneration (GA)	0	1	0	0
rs6931865	4E-6	5.39794000867204	22704111	Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.	Erectile dysfunction	1	1	1	1
rs950146	4E-6	5.39794000867204	22704111	Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.	Erectile dysfunction	1	1	1	1
rs11880316	4E-6	5.39794000867204	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Estradiol levels	1	1	1	1
rs17056274	4E-6	5.39794000867204	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Estradiol levels	1	1	1	1
rs9905820	4E-6	5.39794000867204	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Testosterone levels	1	1	1	1
rs6482992	4E-6	5.39794000867204	22658654	Genomic determinants of motor and cognitive outcomes in Parkinson's disease.	Parkinson's disease (motor and cognition)	1	1	1	1
rs11121382	4E-6	5.39794000867204	22658931	A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed.	Immune response to anthrax vaccine 	1	1	1	1
rs634308	4E-6	5.39794000867204	22658931	A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed.	Immune response to anthrax vaccine 	1	1	1	1
rs9635542	4E-6	5.39794000867204	22637743	Genome-wide gene-environment interaction analysis for asbestos exposure in lung cancer susceptibility.	Lung cancer-asbestos exposure interaction	1	1	1	1
rs2833693	4E-6	5.39794000867204	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	1	1	1	1
rs990871	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	0	1	1	1
rs2324999	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	0	0	0	0
rs1453160	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs1299548	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs2287654	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs2842895	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	0	1	1	1
rs10120372	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	1	1	1
rs2943640	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	1	1	1
rs6124878	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs1056053	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs9899891	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs8013477	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs1536827	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs16910421	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs11839514	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs1411916	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs326155	4E-6	5.39794000867204	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs12125250	4E-6	5.39794000867204	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs1850744	4E-6	5.39794000867204	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs1682825	4E-6	5.39794000867204	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (feminism/equality)	1	1	1	1
rs7235528	4E-6	5.39794000867204	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	0	0	0	0
rs11969893	4E-6	5.39794000867204	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	0	0	0	0
rs3789119	4E-6	5.39794000867204	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	0	1	1	1
rs1539909	4E-6	5.39794000867204	22569225	Investigation of single nucleotide polymorphisms and biological pathways associated with response to TNFα inhibitors in patients with rheumatoid arthritis.	Response to TNF-alpha inhibitors in rheumatoid arthritis	1	1	1	1
rs3794271	4E-6	5.39794000867204	22569225	Investigation of single nucleotide polymorphisms and biological pathways associated with response to TNFα inhibitors in patients with rheumatoid arthritis.	Response to TNF-alpha inhibitors in rheumatoid arthritis	0	0	0	0
rs6867913	4E-6	5.39794000867204	22561531	Genome-wide association study to identify genetic determinants of severe asthma.	Asthma	0	1	1	1
rs10970976	4E-6	5.39794000867204	22561531	Genome-wide association study to identify genetic determinants of severe asthma.	Asthma	0	1	1	1
rs16984547	4E-6	5.39794000867204	22561531	Genome-wide association study to identify genetic determinants of severe asthma.	Asthma	1	1	1	1
rs9860340	4E-6	5.39794000867204	22554406	Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6.	Electroencephalographic traits in alcoholism	1	1	1	1
rs11655470	4E-6	5.39794000867204	22504419	Common variants at 12q15 and 12q24 are associated with infant head circumference.	Head circumference (infant)	0	1	1	1
rs1051920	4E-6	5.39794000867204	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	0	1	1	1
rs4716055	4E-6	5.39794000867204	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	1	1	1	1
rs10885531	4E-6	5.39794000867204	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	1	1	1
rs601339	4E-6	5.39794000867204	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	1	1	1	1
rs3741920	4E-6	5.39794000867204	22437554	Genome-wide association study identifies three common variants associated with serologic response to vitamin E supplementation in men.	Response to Vitamin E supplementation	1	1	1	1
rs17623382	4E-6	5.39794000867204	22437554	Genome-wide association study identifies three common variants associated with serologic response to vitamin E supplementation in men.	Response to Vitamin E supplementation	1	1	1	1
rs2607292	4E-6	5.39794000867204	22446040	A novel locus for body mass index on 5p15.2: a meta-analysis of two genome-wide association studies.	Body mass index	0	0	0	0
rs17077331	4E-6	5.39794000867204	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs2658782	4E-6	5.39794000867204	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs11686135	4E-6	5.39794000867204	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs6070346	4E-6	5.39794000867204	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs2150410	4E-6	5.39794000867204	22365631	Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.	Temperament (bipolar disorder)	1	1	1	1
rs17121944	4E-6	5.39794000867204	22365631	Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.	Temperament (bipolar disorder)	1	1	1	1
rs4513299	4E-6	5.39794000867204	22228203	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Inflammatory biomarkers	1	1	1	1
rs12570947	4E-6	5.39794000867204	22210626	Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.	Prion diseases	1	1	1	1
rs2979481	4E-6	5.39794000867204	22174390	Heritability of submaximal exercise heart rate response to exercise training is accounted for by nine SNPs.	Heart rate variability traits	1	1	1	1
rs2342371	4E-6	5.39794000867204	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	1	1	1	1
rs7523050	4E-6	5.39794000867204	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	0	0	0	0
rs3827730	4E-6	5.39794000867204	22064162	Genome-wide association study of comorbid depressive syndrome and alcohol dependence.	Depression and alcohol dependence	1	1	1	1
rs8111589	4E-6	5.39794000867204	22064162	Genome-wide association study of comorbid depressive syndrome and alcohol dependence.	Depression and alcohol dependence	1	1	1	1
rs2282335	4E-6	5.39794000867204	22044751	Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study.	Renal sinus fat 	1	1	1	1
rs6586513	4E-6	5.39794000867204	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	Allergic rhinitis	1	1	1	1
rs2810114	4E-6	5.39794000867204	22004471	Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.	Alcohol dependence	1	1	1	1
rs10517270	4E-6	5.39794000867204	22005931	Genome-wide association analysis of age-at-onset in Alzheimer's disease.	Alzheimer's disease (age of onset)	1	1	1	1
rs2034764	4E-6	5.39794000867204	22005931	Genome-wide association analysis of age-at-onset in Alzheimer's disease.	Alzheimer's disease (age of onset)	1	1	1	1
rs2659546	4E-6	5.39794000867204	21979947	A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.	Corneal structure	1	1	1	1
rs9310995	4E-6	5.39794000867204	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	1	1	1
rs3734729	4E-6	5.39794000867204	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs2176528	4E-6	5.39794000867204	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	1	1	1	1
rs445925	4E-6	5.39794000867204	21909108	Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.	Carotid intima media thickness	0	0	0	0
rs2384550	4E-6	5.39794000867204	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs8062326	4E-6	5.39794000867204	21876473	Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder.	Alcohol dependence	1	1	1	1
rs12456021	4E-6	5.39794000867204	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs6952809	4E-6	5.39794000867204	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs17594362	4E-6	5.39794000867204	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs386965	4E-6	5.39794000867204	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs9821630	4E-6	5.39794000867204	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs11162963	4E-6	5.39794000867204	21782286	A genome-wide association study of aging.	Aging (time to event)	1	1	1	1
rs12037173	4E-6	5.39794000867204	21784300	Genome-wide association study of the child behavior checklist dysregulation profile.	Attention deficit hyperactivity disorder	1	1	1	1
rs11607165	4E-6	5.39794000867204	21784300	Genome-wide association study of the child behavior checklist dysregulation profile.	Attention deficit hyperactivity disorder	0	0	0	0
rs1059440	4E-6	5.39794000867204	21784300	Genome-wide association study of the child behavior checklist dysregulation profile.	Attention deficit hyperactivity disorder	0	0	0	0
rs13252298	4E-6	5.39794000867204	21743057	Genome-wide association study identifies new prostate cancer susceptibility loci.	Prostate cancer	0	0	0	0
rs8111071	4E-6	5.39794000867204	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs732577	4E-6	5.39794000867204	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs13007495	4E-6	5.39794000867204	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs12644284	4E-6	5.39794000867204	21654844	Genome-wide association study of severity in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs1341239	4E-6	5.39794000867204	21623375	Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.	Paget's disease	1	1	1	1
rs12188164	4E-6	5.39794000867204	21602797	Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.	Cystic fibrosis severity	1	1	1	1
rs7217319	4E-6	5.39794000867204	21502085	Genome-wide association study implicates PARD3B-based AIDS restriction.	AIDS progression	1	1	1	1
rs2140418	4E-6	5.39794000867204	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (alcohol dependence factor score)	0	1	1	1
rs2140418	4E-6	5.39794000867204	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (alcohol use disorder factor score)	0	1	0	0
rs9466056	4E-6	5.39794000867204	21533022	Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.	Bone mineral density	0	1	1	1
rs9594738	4E-6	5.39794000867204	21533022	Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.	Bone mineral density	0	1	1	1
rs6712720	4E-6	5.39794000867204	21493818	Genetic and clinical correlates of early-outgrowth colony-forming units.	Monocyte early outgrowth colony forming units	1	1	1	1
rs1991867	4E-6	5.39794000867204	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	1	1	1	1
rs867186	4E-6	5.39794000867204	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	0	1	1	1
rs7442317	4E-6	5.39794000867204	21473668	Genome-wide association study of motor coordination problems in ADHD identifies genes for brain and muscle function.	Attention deficit hyperactivity disorder motor coordination	1	1	1	1
rs2698530	4E-6	5.39794000867204	21483845	Genome-wide association study identifies genetic loci associated with iron deficiency.	Iron status biomarkers	0	0	0	0
rs1342038	4E-6	5.39794000867204	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs6702784	4E-6	5.39794000867204	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs6593122	4E-6	5.39794000867204	21396408	Atopy history and the genomics of wheezing after influenza vaccination in children 6-59 months of age.	Vaccine-related adverse events 	1	1	1	1
rs10437629	4E-6	5.39794000867204	21423239	A genome-wide association study of attempted suicide.	Suicide attempts in bipolar disorder	1	1	1	1
rs6695567	4E-6	5.39794000867204	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	1	1	1	1
rs4963128	4E-6	5.39794000867204	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	0	0	1	1
rs12629106	4E-6	5.39794000867204	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	1	1	1	1
rs10876993	4E-6	5.39794000867204	21383967	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Celiac disease and Rheumatoid arthritis	0	1	1	1
rs3738443	4E-6	5.39794000867204	21314694	Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.	Alcohol dependence	1	1	1	1
rs4739466	4E-6	5.39794000867204	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs6574988	4E-6	5.39794000867204	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	0	1	1	1
rs4236016	4E-6	5.39794000867204	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	NA	NA	NA	NA
rs4869419	4E-6	5.39794000867204	21273288	Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster.	Natriuretic peptide levels	1	1	1	1
rs6922632	4E-6	5.39794000867204	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs16939046	4E-6	5.39794000867204	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs10510837	4E-6	5.39794000867204	21182207	Variants in several genomic regions associated with asperger disorder.	Asperger disorder	1	1	1	1
rs9871760	4E-6	5.39794000867204	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	MRI atrophy measures	1	1	1	1
rs368331	4E-6	5.39794000867204	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	MRI atrophy measures	0	1	0	0
rs17552189	4E-6	5.39794000867204	21668797	A genome-wide association study of DSM-IV cannabis dependence.	Cannabis dependence	0	1	1	1
rs11579964	4E-6	5.39794000867204	21042317	Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned.	Major depressive disorder	1	1	1	1
rs9501030	4E-6	5.39794000867204	20848476	Genetic predictors of medically refractory ulcerative colitis.	Ulcerative colitis	0	1	1	1
rs6059101	4E-6	5.39794000867204	20848476	Genetic predictors of medically refractory ulcerative colitis.	Ulcerative colitis	1	1	1	1
rs992564	4E-6	5.39794000867204	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs4143844	4E-6	5.39794000867204	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs17002034	4E-6	5.39794000867204	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs7533906	4E-6	5.39794000867204	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs7319311	4E-6	5.39794000867204	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs10929808	4E-6	5.39794000867204	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1106634	4E-6	5.39794000867204	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs11097407	4E-6	5.39794000867204	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs13064588	4E-6	5.39794000867204	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1410530	4E-6	5.39794000867204	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	NA	NA	NA	NA
rs4006360	4E-6	5.39794000867204	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs8170	4E-6	5.39794000867204	20852633	Common variants at 19p13 are associated with susceptibility to ovarian cancer.	Ovarian cancer	0	0	0	0
rs7159300	4E-6	5.39794000867204	20811658	Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement.	Smoking cessation	1	1	1	1
rs4982029	4E-6	5.39794000867204	20713499	Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression.	Schizophrenia, bipolar disorder and depression (combined)	1	1	1	1
rs2049953	4E-6	5.39794000867204	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (AST)	1	1	1	1
rs2216228	4E-6	5.39794000867204	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (lobular)	1	1	1	1
rs7632299	4E-6	5.39794000867204	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (lobular)	1	1	1	1
rs11669592	4E-6	5.39794000867204	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs2358462	4E-6	5.39794000867204	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	0	1	1	1
rs10492294	4E-6	5.39794000867204	20694011	Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.	Immunoglobulin A 	0	1	1	1
rs4131099	4E-6	5.39794000867204	20691247	A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality.	Personality dimensions	1	1	1	1
rs3120665	4E-6	5.39794000867204	20691247	A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality.	Personality dimensions	0	1	1	1
rs2357266	4E-6	5.39794000867204	20707712	A genome-wide association study of self-rated health.	Self-rated health	1	1	1	1
rs1890645	4E-6	5.39794000867204	20662065	Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus.	Neonatal lupus	1	1	1	1
rs4760790	4E-6	5.39794000867204	20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Type 2 diabetes	0	0	1	1
rs2841498	4E-6	5.39794000867204	20522523	Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.	Partial epilepsies	1	1	1	1
rs438259	4E-6	5.39794000867204	20732626	Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	1	1	1	1
rs2602381	4E-6	5.39794000867204	20732626	Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	0	1	1	1
rs11203203	4E-6	5.39794000867204	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs3890745	4E-6	5.39794000867204	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	0	1	1
rs7687921	4E-6	5.39794000867204	20400778	Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.	Mortality among heart failure patients	1	1	1	1
rs10237118	4E-6	5.39794000867204	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (cup)	1	1	1	1
rs17111394	4E-6	5.39794000867204	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (rim)	1	1	1	1
rs11878133	4E-6	5.39794000867204	20385819	Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.	Age-related macular degeneration	1	1	1	1
rs1013696	4E-6	5.39794000867204	20360315	Genome-wide pharmacogenetics of antidepressant response in the GENDEP project.	Response to antidepressants	1	1	1	1
rs7226677	4E-6	5.39794000867204	20351715	Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.	Bipolar disorder and major depressive disorder (combined)	1	1	1	1
rs2053302	4E-6	5.39794000867204	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs646776	4E-6	5.39794000867204	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	0	1	1	1
rs6070116	4E-6	5.39794000867204	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs3757057	4E-6	5.39794000867204	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs13106227	4E-6	5.39794000867204	20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Eosinophilic esophagitis (pediatric)	0	0	0	0
rs9832461	4E-6	5.39794000867204	20197096	Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.	Brain structure (temporal lobe volume)	1	1	1	1
rs12424086	4E-6	5.39794000867204	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (number of teeth)	0	0	1	1
rs10517437	4E-6	5.39794000867204	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs492478	4E-6	5.39794000867204	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs10455248	4E-6	5.39794000867204	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs2616984	4E-6	5.39794000867204	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs4751674	4E-6	5.39794000867204	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs10879517	4E-6	5.39794000867204	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs1265879	4E-6	5.39794000867204	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	0	0	0	0
rs530501	4E-6	5.39794000867204	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	NA	NA	NA	NA
rs10514718	4E-6	5.39794000867204	20125088	Genome-wide association study of recurrent early-onset major depressive disorder.	Major depressive disorder	1	1	1	1
rs16864755	4E-6	5.39794000867204	20200953	Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study.	Osteoporosis-related phenotypes	1	1	1	1
rs783540	4E-6	5.39794000867204	20062064	Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk.	Chronic lymphocytic leukemia	0	1	1	1
rs1326986	4E-6	5.39794000867204	20062062	Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.	Ankylosing spondylitis	1	1	1	1
rs17027625	4E-6	5.39794000867204	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs1385351	4E-6	5.39794000867204	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs6840361	4E-6	5.39794000867204	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	1	1	1	1
rs908922	4E-6	5.39794000867204	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	0	1	1	1
rs3124314	4E-6	5.39794000867204	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	0	0	0	0
rs7919006	4E-6	5.39794000867204	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Weight	1	1	1	1
rs10844154	4E-6	5.39794000867204	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Weight	0	1	1	1
rs9303521	4E-6	5.39794000867204	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (hip)	0	1	0	0
rs228769	4E-6	5.39794000867204	19801982	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.	Bone mineral density (spine)	0	1	0	0
rs1941184	4E-6	5.39794000867204	19772629	Genomewide association study for onset age in Parkinson disease.	Parkinson's disease (age of onset)	1	1	1	1
rs10800098	4E-6	5.39794000867204	19754311	Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03).	AIDS	0	1	1	1
rs3108919	4E-6	5.39794000867204	19754311	Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03).	AIDS	1	1	1	1
rs7612209	4E-6	5.39794000867204	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs2124349	4E-6	5.39794000867204	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs6683071	4E-6	5.39794000867204	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	0	1	1	1
rs816488	4E-6	5.39794000867204	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs10810865	4E-6	5.39794000867204	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs4258076	4E-6	5.39794000867204	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs10887741	4E-6	5.39794000867204	19727025	Genome-wide association study of exercise behavior in Dutch and American adults.	Exercise (leisure time)	0	1	1	1
rs10873876	4E-6	5.39794000867204	19684603	Germline genomic variants associated with childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs10496166	4E-6	5.39794000867204	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs3110127	4E-6	5.39794000867204	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	0	1	1	1
rs1447537	4E-6	5.39794000867204	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs13300284	4E-6	5.39794000867204	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	0	0	0	0
rs5757949	4E-6	5.39794000867204	19570815	A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.	Height	0	0	0	0
rs1572299	4E-6	5.39794000867204	19571808	Common variants conferring risk of schizophrenia.	Schizophrenia	0	1	1	1
rs12388359	4E-6	5.39794000867204	19581569	Genome-wide association study of alcohol dependence.	Alcohol dependence	NA	NA	NA	NA
rs12295638	4E-6	5.39794000867204	19553259	Common body mass index-associated variants confer risk of extreme obesity.	Obesity (extreme)	1	1	1	1
rs374748	4E-6	5.39794000867204	19553259	Common body mass index-associated variants confer risk of extreme obesity.	Obesity (extreme)	1	1	1	1
rs1435703	4E-6	5.39794000867204	19553259	Common body mass index-associated variants confer risk of extreme obesity.	Obesity (extreme)	0	1	1	1
rs4984390	4E-6	5.39794000867204	19483685	HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin.	Drug-induced liver injury (flucloxacillin)	1	1	1	1
rs10848911	4E-6	5.39794000867204	19478329	Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia.	Male infertility	1	1	1	1
rs697739	4E-6	5.39794000867204	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs3177980	4E-6	5.39794000867204	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	NA	NA	NA	NA
rs11775334	4E-6	5.39794000867204	19430479	Genome-wide association study of blood pressure and hypertension.	Hypertension	0	1	1	1
rs2537859	4E-6	5.39794000867204	19416921	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.	Bipolar disorder	1	1	1	1
rs1812175	4E-6	5.39794000867204	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs32579	4E-6	5.39794000867204	19340012	Genome-wide association study of tanning phenotype in a population of European ancestry.	Tanning	1	1	1	1
rs7158173	4E-6	5.39794000867204	19260139	Genome-wide association study of anthropometric traits in Korcula Island, Croatia.	Anthropometric traits	1	1	1	1
rs157350	4E-6	5.39794000867204	19260139	Genome-wide association study of anthropometric traits in Korcula Island, Croatia.	Anthropometric traits	1	1	1	1
rs7792939	4E-6	5.39794000867204	19260139	Genome-wide association study of anthropometric traits in Korcula Island, Croatia.	Anthropometric traits	1	1	1	1
rs2901286	4E-6	5.39794000867204	19176441	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.	Response to treatment for acute lymphoblastic leukemia	1	1	1	1
rs12216125	4E-6	5.39794000867204	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	0	0	0
rs11898505	4E-6	5.39794000867204	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (spine)	0	0	1	1
rs4670779	4E-6	5.39794000867204	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (spine)	1	1	1	1
rs10783050	4E-6	5.39794000867204	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Body mass index	0	0	0	0
rs174570	4E-6	5.39794000867204	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	HDL cholesterol	0	0	0	0
rs8047014	4E-6	5.39794000867204	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	1	1	1	1
rs9845475	4E-6	5.39794000867204	18937294	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.	Attention deficit hyperactivity disorder (time to onset)	1	1	1	1
rs874426	4E-6	5.39794000867204	18937294	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.	Attention deficit hyperactivity disorder (time to onset)	1	1	1	1
rs363512	4E-6	5.39794000867204	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Hyperactive-impulsive symptoms	1	1	1	1
rs8041675	4E-6	5.39794000867204	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Hyperactive-impulsive symptoms	1	1	1	1
rs7172689	4E-6	5.39794000867204	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	1	1	1	1
rs10227331	4E-6	5.39794000867204	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	1	1	1	1
rs9836484	4E-6	5.39794000867204	19023125	A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype.	Brain imaging in schizophrenia (interaction)	1	1	1	1
rs1574192	4E-6	5.39794000867204	19023125	A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype.	Brain imaging in schizophrenia (interaction)	1	1	1	1
rs2602397	4E-6	5.39794000867204	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Brain lesion load	NA	NA	NA	NA
rs1557351	4E-6	5.39794000867204	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (age of onset)	1	1	1	1
rs299175	4E-6	5.39794000867204	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (severity)	0	1	1	1
rs10259085	4E-6	5.39794000867204	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (severity)	0	1	1	1
rs10518025	4E-6	5.39794000867204	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (severity)	1	1	1	1
rs261902	4E-6	5.39794000867204	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Normalized brain volume	0	1	1	1
rs2165738	4E-6	5.39794000867204	18978792	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.	Type 1 diabetes	1	1	1	1
rs402710	4E-6	5.39794000867204	18978790	Lung cancer susceptibility locus at 5p15.33.	Lung cancer	0	0	1	1
rs701157	4E-6	5.39794000867204	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs6733379	4E-6	5.39794000867204	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs7297018	4E-6	5.39794000867204	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs4533251	4E-6	5.39794000867204	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs9803659	4E-6	5.39794000867204	18940312	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.	Liver enzyme levels	1	1	1	1
rs8035957	4E-6	5.39794000867204	18840781	Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs16928529	4E-6	5.39794000867204	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs515910	4E-6	5.39794000867204	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs1555322	4E-6	5.39794000867204	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	0	1	1	1
rs42041	4E-6	5.39794000867204	18794853	Common variants at CD40 and other loci confer risk of rheumatoid arthritis.	Rheumatoid arthritis	0	1	1	1
rs4750316	4E-6	5.39794000867204	18794853	Common variants at CD40 and other loci confer risk of rheumatoid arthritis.	Rheumatoid arthritis	0	0	1	1
rs17065323	4E-6	5.39794000867204	18759275	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish.	Uric acid levels	1	1	1	1
rs12290811	4E-6	5.39794000867204	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	0	0	1	1
rs17082664	4E-6	5.39794000867204	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	0	0	1	1
rs16966460	4E-6	5.39794000867204	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	1	1	1	1
rs4380451	4E-6	5.39794000867204	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	0	0	1	1
rs216345	4E-6	5.39794000867204	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	0	1	1	1
rs1398024	4E-6	5.39794000867204	18723019	Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2.	Crohn's disease and sarcoidosis (combined)	1	1	1	1
rs13393173	4E-6	5.39794000867204	18615156	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.	Response to TNF antagonist treatment	1	1	1	1
rs437943	4E-6	5.39794000867204	18615156	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.	Response to TNF antagonist treatment	1	1	1	1
rs10191411	4E-6	5.39794000867204	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	1	1	1
rs9834373	4E-6	5.39794000867204	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs9461688	4E-6	5.39794000867204	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	1	1	1
rs4770433	4E-6	5.39794000867204	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs9487094	4E-6	5.39794000867204	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs9472138	4E-6	5.39794000867204	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	0	1	1	1
rs979233	4E-6	5.39794000867204	18204098	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.	Systemic lupus erythematosus	1	1	1	1
rs8005745	4E-6	5.39794000867204	17903293	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Select biomarker traits	1	1	1	1
rs10492604	4E-6	5.39794000867204	17903308	Genome-wide association of sleep and circadian phenotypes.	Sleep duration	1	1	1	1
rs6977660	4E-6	5.39794000867204	17903292	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.	Thyroid stimulating hormone	1	1	1	1
rs2053506	4E-6	5.39794000867204	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	1	1	1	1
rs638882	4E-6	5.39794000867204	17903296	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	Hip geometry	1	1	1	1
rs4370013	4E-6	5.39794000867204	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Blood pressure	1	1	1	1
rs10491334	4E-6	5.39794000867204	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Blood pressure	0	1	1	1
rs10521232	4E-6	5.39794000867204	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Tonometry	1	1	1	1
rs3766680	4E-6	5.39794000867204	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Tonometry	1	1	1	1
rs1371924	4E-6	5.39794000867204	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Tonometry	1	1	1	1
rs530965	4E-6	5.39794000867204	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Cognitive test performance	0	1	1	1
rs2819770	4E-6	5.39794000867204	17903301	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	Exercise treadmill test traits	1	1	1	1
rs10516541	4E-6	5.39794000867204	17903307	Framingham Heart Study genome-wide association: results for pulmonary function measures.	Mean forced vital capacity from 2 exams	1	1	1	1
rs1455782	4E-6	5.39794000867204	17903307	Framingham Heart Study genome-wide association: results for pulmonary function measures.	Pulmonary function	1	1	1	1
rs565229	4E-6	5.39794000867204	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs9253	4E-6	5.39794000867204	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs6498169	4E-6	5.39794000867204	17660530	Risk alleles for multiple sclerosis identified by a genomewide study.	Multiple sclerosis	0	0	1	1
rs6458307	4E-6	5.39794000867204	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Bipolar disorder	1	1	1	1
rs688034	4E-6	5.39794000867204	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Coronary heart disease	1	1	1	1
rs7807268	4E-6	5.39794000867204	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Crohn's disease	1	1	1	1
rs2555155	5E-6	5.30102999566398	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	1	1	1	1
rs10462794	5E-6	5.30102999566398	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	1	1	1	1
rs4304977	5E-6	5.30102999566398	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	1	1	1	1
rs10823607	5E-6	5.30102999566398	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep duration	1	1	1	1
rs2278331	5E-6	5.30102999566398	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep duration	1	1	1	1
rs9836672	5E-6	5.30102999566398	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep quality	1	1	1	1
rs8081523	5E-6	5.30102999566398	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Se levels)	1	1	1	1
rs6586282	5E-6	5.30102999566398	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Se levels)	0	1	1	1
rs10931753	5E-6	5.30102999566398	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Zn levels)	1	1	1	1
rs6793516	5E-6	5.30102999566398	23720494	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Blood trace element (Zn levels)	NA	NA	NA	NA
rs9951026	5E-6	5.30102999566398	23666239	Meta-analysis identifies four new loci associated with testicular germ cell tumor.	Testicular germ cell tumor	1	1	1	1
rs8005845	5E-6	5.30102999566398	23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Body mass index	1	1	1	1
rs3936060	5E-6	5.30102999566398	23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Body mass index	0	0	1	1
rs7158359	5E-6	5.30102999566398	23643386	Weight loss after gastric bypass is associated with a variant at 15q26.1.	Weight loss (gastric bypass surgery)	1	1	1	1
rs2840445	5E-6	5.30102999566398	23636237	Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake.	Dietary macronutrient intake	1	1	1	1
rs8019546	5E-6	5.30102999566398	23636237	Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake.	Dietary macronutrient intake	1	1	1	1
rs955943	5E-6	5.30102999566398	23585552	Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.	Rhegmatogenous retinal detachment	1	1	1	1
rs56148675	5E-6	5.30102999566398	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs2221433	5E-6	5.30102999566398	23568457	Genetic variants associated with disordered eating.	Eating disorders	1	1	1	1
rs514024	5E-6	5.30102999566398	23568457	Genetic variants associated with disordered eating.	Eating disorders (purging via substances) 	1	1	1	1
rs8113142	5E-6	5.30102999566398	23593202	Bivariate genome-wide association analyses identified genes with pleiotropic effects for femoral neck bone geometry and age at menarche.	Femoral neck bone geometry and menarche (age at onset)	0	0	0	0
rs8099213	5E-6	5.30102999566398	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs9311745	5E-6	5.30102999566398	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Pit-and-Fissure caries 	1	1	1	1
rs1612141	5E-6	5.30102999566398	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	1	1	1	1
rs10916248	5E-6	5.30102999566398	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	1	1	1	1
rs2663905	5E-6	5.30102999566398	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	1	1	1	1
rs3118906	5E-6	5.30102999566398	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs1107592	5E-6	5.30102999566398	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs6765687	5E-6	5.30102999566398	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	0	0	0
rs10255295	5E-6	5.30102999566398	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs11731175	5E-6	5.30102999566398	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs7799006	5E-6	5.30102999566398	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	0	0	0
rs363598	5E-6	5.30102999566398	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs2675968	5E-6	5.30102999566398	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs703970	5E-6	5.30102999566398	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs7948661	5E-6	5.30102999566398	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs17011455	5E-6	5.30102999566398	23509613	Genome-wide association study of antiphospholipid antibodies.	Presence of antiphospholipid antibodies	1	1	1	1
rs3017493	5E-6	5.30102999566398	23432519	A genome-wide association study of recipient genotype and medium-term kidney allograft function.	Renal transplant outcome	1	1	1	1
rs17638544	5E-6	5.30102999566398	23437003	Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure.	Bone mineral density	0	0	1	1
rs4669226	5E-6	5.30102999566398	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs12513380	5E-6	5.30102999566398	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs9472138	5E-6	5.30102999566398	23408906	A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.	Thyroid hormone levels	0	0	0	0
rs10004839	5E-6	5.30102999566398	23393555	Genome-wide association study of retinopathy in individuals without diabetes.	Retinopathy in non-diabetics	1	1	1	1
rs9918807	5E-6	5.30102999566398	23393555	Genome-wide association study of retinopathy in individuals without diabetes.	Retinopathy in non-diabetics	1	1	1	1
rs17203055	5E-6	5.30102999566398	23894747	A comprehensive family-based replication study of schizophrenia genes.	Schizophrenia	1	1	1	1
rs166040	5E-6	5.30102999566398	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs398426	5E-6	5.30102999566398	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	0	0	0	0
rs12465996	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4875857	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6969802	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11710456	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1953652	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11994937	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2833991	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11212260	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6065945	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7895244	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs3097645	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1174864	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs980952	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6853847	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs871012	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6132333	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7032871	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7623788	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs13328933	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7331540	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2430457	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs12207186	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11700462	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1739654	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs17594709	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs6102185	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs12772243	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs13178541	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4710520	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11765886	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs404256	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6084946	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10236237	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2163237	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs4730268	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6787231	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2577704	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11188352	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2110166	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2184180	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs586446	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7661864	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9886428	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2094962	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs13295552	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2140930	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10069748	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11079764	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10903027	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4899329	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11675841	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs435066	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6059594	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2090104	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2080501	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs9284954	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs139014	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9492645	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11568995	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs5764106	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7325564	5E-6	5.30102999566398	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs17177078	5E-6	5.30102999566398	23386860	Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes.	Type 2 diabetes (dietary heme iron intake interaction)	1	1	1	1
rs2981205	5E-6	5.30102999566398	23358156	Childhood intelligence is heritable, highly polygenic and associated with FNBP1L.	Intelligence (childhood)	1	1	1	1
rs4757144	5E-6	5.30102999566398	23358160	Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.	Schizophrenia	0	1	1	1
rs4731889 	5E-6	5.30102999566398	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Oleic acid (18:1n-9) plasma levels	NA	NA	NA	NA
rs17774576 	5E-6	5.30102999566398	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Oleic acid (18:1n-9) plasma levels	NA	NA	NA	NA
rs11006464 	5E-6	5.30102999566398	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Oleic acid (18:1n-9) plasma levels	NA	NA	NA	NA
rs9816269 	5E-6	5.30102999566398	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitic acid (16:0) plasma levels	NA	NA	NA	NA
rs12297524 	5E-6	5.30102999566398	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitic acid (16:0) plasma levels	NA	NA	NA	NA
rs7597155 	5E-6	5.30102999566398	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Palmitoleic acid (16:1n-7) plasma levels	NA	NA	NA	NA
rs7550711 	5E-6	5.30102999566398	23362303	Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	Stearic acid (18:0) plasma levels	NA	NA	NA	NA
rs7453920	5E-6	5.30102999566398	23349640	Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.	Lymphoma	0	0	0	0
rs7147503	5E-6	5.30102999566398	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs4655303	5E-6	5.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA)	1	1	1	1
rs7047865	5E-6	5.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA)	1	1	1	1
rs9357377	5E-6	5.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA/ MHPG Ratio)	1	1	1	1
rs6526555	5E-6	5.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA/ MHPG Ratio)	NA	NA	NA	NA
rs7029536	5E-6	5.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA)	0	1	1	1
rs9619497	5E-6	5.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA-5-HIAA Factor score)	1	1	1	1
rs35593266	5E-6	5.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/5-HIAA ratio)	0	1	1	1
rs56240109	5E-6	5.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/5-HIAA ratio)	1	1	1	1
rs4845812	5E-6	5.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs1158058	5E-6	5.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs1925265	5E-6	5.30102999566398	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	NA	NA	NA	NA
rs16851585	5E-6	5.30102999566398	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	1	1	1	1
rs1967689	5E-6	5.30102999566398	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	1	1	1
rs11986011	5E-6	5.30102999566398	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	NA	NA	NA	NA
rs1867631	5E-6	5.30102999566398	23307926	A genome-wide association study of early menopause and the combined impact of identified variants.	Menopause (age at onset)	1	1	1	1
rs4888966	5E-6	5.30102999566398	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs9961915	5E-6	5.30102999566398	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs2832191	5E-6	5.30102999566398	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	0	1	1	1
rs3204270	5E-6	5.30102999566398	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs7634533	5E-6	5.30102999566398	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	0	1	1	1
rs172166	5E-6	5.30102999566398	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	0	1	1	1
rs1526687	5E-6	5.30102999566398	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	1	1	1	1
rs2201728	5E-6	5.30102999566398	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	0	1	1	1
rs12743824	5E-6	5.30102999566398	23213074	Association between liver-specific gene polymorphisms and their expression levels with nonalcoholic fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs5415	5E-6	5.30102999566398	23202124	New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.	Birth weight	0	1	1	1
rs4530903	5E-6	5.30102999566398	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	0	1	1	1
rs7006821	5E-6	5.30102999566398	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	1	1	1	1
rs7147624	5E-6	5.30102999566398	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	1	1	1
rs1260326	5E-6	5.30102999566398	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity and mass	0	1	1	1
rs10255295	5E-6	5.30102999566398	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	0	1	1	1
rs1775715	5E-6	5.30102999566398	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	1	1	1	1
rs2962370	5E-6	5.30102999566398	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	1	1	1	1
rs11256676	5E-6	5.30102999566398	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs649057	5E-6	5.30102999566398	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs6683977	5E-6	5.30102999566398	23007406	Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs1496766	5E-6	5.30102999566398	23007406	Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs9958208	5E-6	5.30102999566398	23007406	Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	0	1	1	1
rs6027506	5E-6	5.30102999566398	23028342	New susceptibility loci associated with kidney disease in type 1 diabetes.	Type 1 diabetes nephropathy	0	0	0	0
rs4802666	5E-6	5.30102999566398	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs2484992	5E-6	5.30102999566398	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs9488238	5E-6	5.30102999566398	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs740145	5E-6	5.30102999566398	22969067	Genetic variants near PDGFRA are associated with corneal curvature in Australians.	Corneal curvature	1	1	1	1
rs2383876	5E-6	5.30102999566398	22969067	Genetic variants near PDGFRA are associated with corneal curvature in Australians.	Corneal curvature	1	1	1	1
rs4529888	5E-6	5.30102999566398	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	1	1	1	1
rs2819332	5E-6	5.30102999566398	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis (age of onset)	0	0	0	0
rs669446	5E-6	5.30102999566398	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis (age of onset)	0	0	0	0
rs2904524	5E-6	5.30102999566398	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis (age of onset)	1	1	1	1
rs6738181	5E-6	5.30102999566398	22881374	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	Alzheimer's disease (late onset)	1	1	1	1
rs16869652	5E-6	5.30102999566398	22885689	Genome-wide association study of multiplex schizophrenia pedigrees.	Schizophrenia	1	1	1	1
rs10761659	5E-6	5.30102999566398	22936669	A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.	Crohn's disease	0	0	1	1
rs10237317	5E-6	5.30102999566398	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	1	1	1	1
rs3750552	5E-6	5.30102999566398	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	1	1	1	1
rs2287375	5E-6	5.30102999566398	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	1	1	1	1
rs1557305	5E-6	5.30102999566398	22911880	Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits.	Eating disorders	1	1	1	1
rs6941712	5E-6	5.30102999566398	22903471	Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.	Lentiform nucleus volume 	0	1	1	1
rs2037892	5E-6	5.30102999566398	22903471	Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.	Lentiform nucleus volume 	0	0	0	0
rs1919922	5E-6	5.30102999566398	22903471	Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.	Lentiform nucleus volume 	0	0	0	0
rs9426935	5E-6	5.30102999566398	22903471	Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.	Lentiform nucleus volume 	0	0	0	0
rs11083866	5E-6	5.30102999566398	22903471	Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.	Lentiform nucleus volume 	1	1	1	1
rs2252508	5E-6	5.30102999566398	22903471	Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.	Lentiform nucleus volume 	0	0	0	0
rs10990268	5E-6	5.30102999566398	22889924	Genome-wide association study of Tourette's syndrome.	Tourette syndrome	1	1	1	1
rs9652236	5E-6	5.30102999566398	22889921	Genome-wide association study of obsessive-compulsive disorder.	Obsessive-compulsive disorder	1	1	1	1
rs519595	5E-6	5.30102999566398	22890011	Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate.	Response to fenofibrate	0	0	0	0
rs7950069	5E-6	5.30102999566398	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs12505749	5E-6	5.30102999566398	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs1207393	5E-6	5.30102999566398	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	0	1	1	1
rs4789400	5E-6	5.30102999566398	22823124	The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation.	Cannabis use (initiation)	1	1	1	1
rs9383153	5E-6	5.30102999566398	22780124	Genome-wide association study of a quantitative disordered gambling trait.	Gambling	1	1	1	1
rs10812227	5E-6	5.30102999566398	22780124	Genome-wide association study of a quantitative disordered gambling trait.	Gambling	0	0	0	0
rs11585386	5E-6	5.30102999566398	22773346	Linkage and association of successful aging to the 6q25 region in large Amish kindreds.	Aging	1	1	1	1
rs16892673	5E-6	5.30102999566398	22773346	Linkage and association of successful aging to the 6q25 region in large Amish kindreds.	Aging	1	1	1	1
rs10830964	5E-6	5.30102999566398	22754043	A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.	Insomnia (caffeine-induced)	1	1	1	1
rs1616122	5E-6	5.30102999566398	22699663	Genome-wide association study of periodontal pathogen colonization.	Periodontal microbiota	1	1	1	1
rs7102705	5E-6	5.30102999566398	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs7837045	5E-6	5.30102999566398	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs780093	5E-6	5.30102999566398	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	0	0	0	0
rs271738	5E-6	5.30102999566398	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder	1	1	1	1
rs289585	5E-6	5.30102999566398	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder	1	1	1	1
rs181500	5E-6	5.30102999566398	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs424950	5E-6	5.30102999566398	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Sex hormone-binding globulin levels	1	1	1	1
rs8077059	5E-6	5.30102999566398	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Sex hormone-binding globulin levels	1	1	1	1
rs17000647	5E-6	5.30102999566398	22658654	Genomic determinants of motor and cognitive outcomes in Parkinson's disease.	Parkinson's disease (motor and cognition)	1	1	1	1
rs959573	5E-6	5.30102999566398	22658654	Genomic determinants of motor and cognitive outcomes in Parkinson's disease.	Parkinson's disease (motor and cognition)	1	1	1	1
rs6856768	5E-6	5.30102999566398	22832961	Genome-wide association study of Alzheimer's disease.	Alzheimer's disease	1	1	1	1
rs11738335	5E-6	5.30102999566398	22832961	Genome-wide association study of Alzheimer's disease.	Alzheimer's disease	1	1	1	1
rs4667682	5E-6	5.30102999566398	22745009	Multiple loci influencing hippocampal degeneration identified by genome scan.	Hippocampal atrophy	1	1	1	1
rs2741200	5E-6	5.30102999566398	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	1	1	1	1
rs12494658	5E-6	5.30102999566398	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	0	1	1	1
rs291272	5E-6	5.30102999566398	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	1	1	1	1
rs1334893	5E-6	5.30102999566398	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	1	1	1	1
rs6013355	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs5743030	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs7525133	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs7120173	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs1316952	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	0	1	0	0
rs11620399	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs12636148	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs6577655	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	1	1	1
rs11620399	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	1	0	0
rs8106493	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	1	0	0
rs2278255	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs1530947	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs11683197	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs11231299	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs3819055	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	NA	NA	NA	NA
rs10772915	5E-6	5.30102999566398	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs10772939	5E-6	5.30102999566398	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs470763	5E-6	5.30102999566398	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (fairness)	1	1	1	1
rs1978633	5E-6	5.30102999566398	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (feminism/equality)	1	1	1	1
rs12606301	5E-6	5.30102999566398	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	0	0	0	0
rs16998084	5E-6	5.30102999566398	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	1	1	1	1
rs4586057	5E-6	5.30102999566398	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (time)	1	1	1	1
rs10748180	5E-6	5.30102999566398	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (time)	1	1	1	1
rs218676	5E-6	5.30102999566398	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (time)	1	1	1	1
rs4804416	5E-6	5.30102999566398	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	0	1	1	1
rs10162002	5E-6	5.30102999566398	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	1	1	1	1
rs1969253	5E-6	5.30102999566398	22472876	A mega-analysis of genome-wide association studies for major depressive disorder.	Major depressive disorder	1	1	1	1
rs4478239	5E-6	5.30102999566398	22472876	A mega-analysis of genome-wide association studies for major depressive disorder.	Major depressive disorder	1	1	1	1
rs9646303	5E-6	5.30102999566398	22472876	A mega-analysis of genome-wide association studies for major depressive disorder.	Major depressive disorder	1	1	1	1
rs9316500	5E-6	5.30102999566398	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	0	1	1	1
rs7006290	5E-6	5.30102999566398	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	0	1	1	1
rs3843306	5E-6	5.30102999566398	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs946836	5E-6	5.30102999566398	22425255	A genome-wide search for genetic influences and biological pathways related to the brain's white matter integrity.	White matter integrity	1	1	1	1
rs285406	5E-6	5.30102999566398	22379998	Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.	Adverse response to lamotrigine and phenytoin	1	1	1	1
rs183266	5E-6	5.30102999566398	22379998	Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.	Adverse response to lamotrigine and phenytoin	1	1	1	1
rs4569005	5E-6	5.30102999566398	22379998	Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.	Adverse response to lamotrigine and phenytoin	1	1	1	1
rs2839398	5E-6	5.30102999566398	22451204	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.	Parkinson's disease	1	1	1	1
rs1865721	5E-6	5.30102999566398	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	1	1	1	1
rs2155929	5E-6	5.30102999566398	22365631	Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.	Temperament (bipolar disorder)	0	1	1	1
rs2603127	5E-6	5.30102999566398	22443383	Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs11856574	5E-6	5.30102999566398	22247754	Genome-wide association of implantable cardioverter-defibrillator activation with life-threatening arrhythmias.	Life threatening arrhythmia	1	1	1	1
rs13358864	5E-6	5.30102999566398	22229870	Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia.	Uric acid levels	1	1	1	1
rs2231142	5E-6	5.30102999566398	22229870	Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia.	Uric acid levels	0	0	1	1
rs7523050	5E-6	5.30102999566398	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	0	0	0	0
rs4417	5E-6	5.30102999566398	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	1	1	1	1
rs4820294	5E-6	5.30102999566398	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	1	1	1	1
rs6074022	5E-6	5.30102999566398	22190364	Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.	Multiple sclerosis	0	0	1	1
rs11242704	5E-6	5.30102999566398	22095909	Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.	Response to hepatitis C treatment	1	1	1	1
rs5922838	5E-6	5.30102999566398	22064162	Genome-wide association study of comorbid depressive syndrome and alcohol dependence.	Depression and alcohol dependence	NA	NA	NA	NA
rs1898671	5E-6	5.30102999566398	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	Allergic rhinitis	0	1	1	1
rs1325195	5E-6	5.30102999566398	22036096	A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.	IgE grass sensitization	1	1	1	1
rs16933812	5E-6	5.30102999566398	22013104	Genome-wide scan for loci of adolescent obesity and their relationship with blood pressure.	Obesity and blood pressure	0	0	0	0
rs1344694	5E-6	5.30102999566398	22004471	Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.	Alcohol dependence	0	0	1	1
rs25422	5E-6	5.30102999566398	22010048	A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23.	Renal cell carcinoma	0	1	1	1
rs2885805	5E-6	5.30102999566398	21993531	Genome-wide association study does not reveal major genetic determinants for anti-cytomegalovirus antibody response.	Cytomegalovirus antibody response	1	1	1	1
rs4766152	5E-6	5.30102999566398	21993531	Genome-wide association study does not reveal major genetic determinants for anti-cytomegalovirus antibody response.	Cytomegalovirus antibody response	0	1	1	1
rs2798641	5E-6	5.30102999566398	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	0	0	0
rs16915157	5E-6	5.30102999566398	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	0	1	1
rs12730292	5E-6	5.30102999566398	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	0	0	1	1
rs699363	5E-6	5.30102999566398	21935397	Genome-wide population-based association study of extremely overweight young adults--the GOYA study.	Obesity (extreme)	1	1	1	1
rs970843	5E-6	5.30102999566398	21935397	Genome-wide population-based association study of extremely overweight young adults--the GOYA study.	Obesity (extreme)	1	1	1	1
rs10745527	5E-6	5.30102999566398	21810271	Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.	vWF and FVIII levels	1	1	1	1
rs6454764	5E-6	5.30102999566398	21810271	Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.	vWF and FVIII levels	1	1	1	1
rs11047102	5E-6	5.30102999566398	21779181	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.	Systemic sclerosis	0	0	0	0
rs10993994	5E-6	5.30102999566398	21743057	Genome-wide association study identifies new prostate cancer susceptibility loci.	Prostate cancer	0	0	1	1
rs13358260	5E-6	5.30102999566398	21700879	Novel locus FER is associated with serum HMW adiponectin levels.	Adiponectin levels	0	1	1	1
rs10517133	5E-6	5.30102999566398	21700879	Novel locus FER is associated with serum HMW adiponectin levels.	Adiponectin levels	1	1	1	1
rs190759	5E-6	5.30102999566398	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	0	1	1	1
rs10219495	5E-6	5.30102999566398	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs10777317	5E-6	5.30102999566398	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs10777845	5E-6	5.30102999566398	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs438034	5E-6	5.30102999566398	21659360	Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial.	Response to antineoplastic agents	1	1	1	1
rs1168987	5E-6	5.30102999566398	21659360	Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial.	Response to antineoplastic agents	1	1	1	1
rs16893526	5E-6	5.30102999566398	21606135	A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.	Coronary heart disease	1	1	1	1
rs6441975	5E-6	5.30102999566398	21502085	Genome-wide association study implicates PARD3B-based AIDS restriction.	AIDS progression	0	1	1	1
rs1109501	5E-6	5.30102999566398	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (heaviness of drinking)	1	1	1	1
rs8014204	5E-6	5.30102999566398	21490707	Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.	Caffeine consumption	0	1	1	1
rs2725236	5E-6	5.30102999566398	21490707	Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.	Caffeine consumption	0	1	1	1
rs3007729	5E-6	5.30102999566398	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs4937126	5E-6	5.30102999566398	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	1	1	1
rs2669010	5E-6	5.30102999566398	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	1	1	1	1
rs12483205	5E-6	5.30102999566398	21364930	Genome-wide association study identifies single nucleotide polymorphism in DYRK1A associated with replication of HIV-1 in monocyte-derived macrophages.	HIV-1 replication	0	1	1	1
rs12020569	5E-6	5.30102999566398	21314694	Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.	Alcohol dependence	NA	NA	NA	NA
rs4903031	5E-6	5.30102999566398	21300955	Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.	C-reactive protein	1	1	1	1
rs17600642	5E-6	5.30102999566398	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs2031532	5E-6	5.30102999566398	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	1	1	1	1
rs17291845	5E-6	5.30102999566398	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs892055	5E-6	5.30102999566398	21182207	Variants in several genomic regions associated with asperger disorder.	Asperger disorder	0	1	1	1
rs2084385	5E-6	5.30102999566398	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	1	1	1	1
rs990324	5E-6	5.30102999566398	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	1	1	1	1
rs12555345	5E-6	5.30102999566398	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	0	1	1	1
rs4662834	5E-6	5.30102999566398	21106707	A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity.	Bleomycin sensitivity	1	1	1	1
rs9427573	5E-6	5.30102999566398	21668797	A genome-wide association study of DSM-IV cannabis dependence.	Cannabis dependence	NA	NA	NA	NA
rs7647854	5E-6	5.30102999566398	21042317	Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned.	Major depressive disorder	0	1	1	1
rs470490	5E-6	5.30102999566398	21041692	Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science.	Atrioventricular conduction	1	1	1	1
rs17166499	5E-6	5.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs10042348	5E-6	5.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1124376	5E-6	5.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs12003180	5E-6	5.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs12321565	5E-6	5.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs12444931	5E-6	5.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1456737	5E-6	5.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	NA	NA	NA	NA
rs17176973	5E-6	5.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs17764205	5E-6	5.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs2367911	5E-6	5.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs4332358	5E-6	5.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs4770837	5E-6	5.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs4870684	5E-6	5.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs5907577	5E-6	5.30102999566398	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	NA	NA	NA	NA
rs7521902	5E-6	5.30102999566398	20852632	A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.	Ovarian cancer	0	1	1	1
rs12794435	5E-6	5.30102999566398	20852632	A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.	Ovarian cancer	1	1	1	1
rs1927745	5E-6	5.30102999566398	20800221	Genome-wide association scan of trait depression.	Depression (quantitative trait)	1	1	1	1
rs10514585	5E-6	5.30102999566398	20800221	Genome-wide association scan of trait depression.	Depression (quantitative trait)	1	1	1	1
rs11009175	5E-6	5.30102999566398	20800221	Genome-wide association scan of trait depression.	Depression (quantitative trait)	1	1	1	1
rs1012036	5E-6	5.30102999566398	20709820	Genome-wide association study identifies BICD1 as a susceptibility gene for emphysema.	Emphysema-related traits	1	1	1	1
rs3847646	5E-6	5.30102999566398	20705733	Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.	Calcium levels	0	1	1	1
rs12344488	5E-6	5.30102999566398	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (AST)	1	1	1	1
rs10067427	5E-6	5.30102999566398	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (lobular)	1	1	1	1
rs9977253	5E-6	5.30102999566398	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs11662763	5E-6	5.30102999566398	20694011	Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.	Immunoglobulin A 	1	1	1	1
rs300489	5E-6	5.30102999566398	20707712	A genome-wide association study of self-rated health.	Self-rated health	1	1	1	1
rs743446	5E-6	5.30102999566398	20662065	Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus.	Neonatal lupus	1	1	1	1
rs1903595	5E-6	5.30102999566398	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	1	1	1	1
rs1490157	5E-6	5.30102999566398	20522523	Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.	Partial epilepsies	1	1	1	1
rs10812610	5E-6	5.30102999566398	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	0	1	1	1
rs12418204	5E-6	5.30102999566398	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (cup)	1	1	1	1
rs1218282	5E-6	5.30102999566398	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	0	1	1	1
rs1992950	5E-6	5.30102999566398	20228799	Genome-wide association identifies multiple ulcerative colitis susceptibility loci.	Ulcerative colitis	1	1	1	1
rs9500256	5E-6	5.30102999566398	20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Eosinophilic esophagitis (pediatric)	1	1	1	1
rs4643574	5E-6	5.30102999566398	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs4450776	5E-6	5.30102999566398	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs17586674	5E-6	5.30102999566398	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs2002030	5E-6	5.30102999566398	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs517811	5E-6	5.30102999566398	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs11166827	5E-6	5.30102999566398	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs448720	5E-6	5.30102999566398	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	0	1	1	1
rs5941436	5E-6	5.30102999566398	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	NA	NA	NA	NA
rs11920090	5E-6	5.30102999566398	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	0	0	0
rs340874	5E-6	5.30102999566398	20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Fasting glucose-related traits	0	0	0	0
rs644695	5E-6	5.30102999566398	20038947	Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.	Major depressive disorder (broad)	0	1	1	1
rs724568	5E-6	5.30102999566398	20038947	Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.	Major depressive disorder (broad)	1	1	1	1
rs7077361	5E-6	5.30102999566398	19915575	Genome-wide association study reveals genetic risk underlying Parkinson's disease.	Parkinson's disease	1	1	1	1
rs1223271	5E-6	5.30102999566398	19915575	Genome-wide association study reveals genetic risk underlying Parkinson's disease.	Parkinson's disease	1	1	1	1
rs3803915	5E-6	5.30102999566398	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Body mass index	1	1	1	1
rs1878047	5E-6	5.30102999566398	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Body mass index	0	1	1	1
rs10501293	5E-6	5.30102999566398	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs2252521	5E-6	5.30102999566398	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs17086609	5E-6	5.30102999566398	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs4601609	5E-6	5.30102999566398	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs12143943	5E-6	5.30102999566398	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	0	1	1	1
rs1082714	5E-6	5.30102999566398	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs4254535	5E-6	5.30102999566398	19654303	Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.	Lung cancer	1	1	1	1
rs744016	5E-6	5.30102999566398	20031603	A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.	RR interval (heart rate)	1	1	1	1
rs36563	5E-6	5.30102999566398	19581569	Genome-wide association study of alcohol dependence.	Alcohol dependence	0	0	1	1
rs7932813	5E-6	5.30102999566398	19557197	NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium.	Waist circumference	1	1	1	1
rs12635698	5E-6	5.30102999566398	19553259	Common body mass index-associated variants confer risk of extreme obesity.	Obesity (extreme)	1	1	1	1
rs10999409	5E-6	5.30102999566398	19553259	Common body mass index-associated variants confer risk of extreme obesity.	Obesity (extreme)	1	1	1	1
rs6110577	5E-6	5.30102999566398	19553259	Common body mass index-associated variants confer risk of extreme obesity.	Obesity (extreme)	1	1	1	1
rs4149584	5E-6	5.30102999566398	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	NA	NA	NA	NA
rs12046278	5E-6	5.30102999566398	19430479	Genome-wide association study of blood pressure and hypertension.	Systolic blood pressure	1	1	1	1
rs7427021	5E-6	5.30102999566398	19416921	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.	Bipolar disorder	1	1	1	1
rs7815788	5E-6	5.30102999566398	19343178	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.	Height	0	0	1	1
rs1402279	5E-6	5.30102999566398	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	1	1	1	1
rs7513590	5E-6	5.30102999566398	19260139	Genome-wide association study of anthropometric traits in Korcula Island, Croatia.	Anthropometric traits	1	1	1	1
rs7792939	5E-6	5.30102999566398	19260139	Genome-wide association study of anthropometric traits in Korcula Island, Croatia.	Anthropometric traits	0	0	0	0
rs10777332	5E-6	5.30102999566398	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	1	1	1	1
rs7128311	5E-6	5.30102999566398	19176441	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.	Response to treatment for acute lymphoblastic leukemia	1	1	1	1
rs35229355	5E-6	5.30102999566398	19176441	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.	Response to treatment for acute lymphoblastic leukemia	1	1	1	1
rs4730273	5E-6	5.30102999566398	19122664	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.	Ulcerative colitis	0	0	0	0
rs2274089	5E-6	5.30102999566398	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	0	0	0
rs1799852	5E-6	5.30102999566398	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	1	1	1
rs1018040	5E-6	5.30102999566398	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	1	1	1	1
rs130575	5E-6	5.30102999566398	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	0	1	1	1
rs1918172	5E-6	5.30102999566398	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	1	1	1	1
rs7992643	5E-6	5.30102999566398	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	1	1	1	1
rs1325154	5E-6	5.30102999566398	18937294	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.	Attention deficit hyperactivity disorder (time to onset)	0	1	1	1
rs6808138	5E-6	5.30102999566398	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Hyperactive-impulsive symptoms	1	1	1	1
rs17641078	5E-6	5.30102999566398	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Hyperactive-impulsive symptoms	1	1	1	1
rs4650135	5E-6	5.30102999566398	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	1	1	1	1
rs17079773	5E-6	5.30102999566398	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	1	1	1	1
rs10133111	5E-6	5.30102999566398	19023125	A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype.	Brain imaging in schizophrenia (interaction)	1	1	1	1
rs2842483	5E-6	5.30102999566398	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (age of onset)	1	1	1	1
rs10229603	5E-6	5.30102999566398	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs931812	5E-6	5.30102999566398	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs1557488	5E-6	5.30102999566398	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs1951082	5E-6	5.30102999566398	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs4964805	5E-6	5.30102999566398	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs2237349	5E-6	5.30102999566398	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs3799977	5E-6	5.30102999566398	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	0	1	1	1
rs719593	5E-6	5.30102999566398	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	1	1	1	1
rs6442522	5E-6	5.30102999566398	18759275	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish.	Uric acid levels	1	1	1	1
rs3821396	5E-6	5.30102999566398	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	1	1	1	1
rs8015959	5E-6	5.30102999566398	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	0	1	1	1
rs12436436	5E-6	5.30102999566398	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	1	1	1	1
rs11720452	5E-6	5.30102999566398	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	1	1	1	1
rs983332	5E-6	5.30102999566398	18615156	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.	Response to TNF antagonist treatment	1	1	1	1
rs763014	5E-6	5.30102999566398	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	0	0	1	1
rs958546	5E-6	5.30102999566398	17903304	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.	Atrial fibrillation	1	1	1	1
rs2121070	5E-6	5.30102999566398	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Blood pressure	0	0	0	0
rs10510634	5E-6	5.30102999566398	17903298	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	Fasting plasma glucose	0	1	1	1
rs180730	5E-6	5.30102999566398	17903298	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	Fasting plasma glucose	1	1	1	1
rs10490113	5E-6	5.30102999566398	17903305	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	Breast cancer	1	1	1	1
rs345013	5E-6	5.30102999566398	17903305	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	Prostate cancer	1	1	1	1
rs2896103	5E-6	5.30102999566398	17903303	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	Subclinical atherosclerosis traits (other)	0	1	1	1
rs9303401	5E-6	5.30102999566398	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Cognitive test performance	0	1	1	1
rs666088	5E-6	5.30102999566398	17903301	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	Echocardiographic traits	1	1	1	1
rs10504543	5E-6	5.30102999566398	17903301	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	Echocardiographic traits	1	1	1	1
rs746463	5E-6	5.30102999566398	17903301	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	Exercise treadmill test traits	1	1	1	1
rs310558	5E-6	5.30102999566398	17903307	Framingham Heart Study genome-wide association: results for pulmonary function measures.	Pulmonary function	1	1	1	1
rs3820928	5E-6	5.30102999566398	17903307	Framingham Heart Study genome-wide association: results for pulmonary function measures.	Pulmonary function	1	1	1	1
rs10506458	5E-6	5.30102999566398	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs10489087	5E-6	5.30102999566398	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs683395	5E-6	5.30102999566398	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Bipolar disorder	0	0	1	1
rs17166496	5E-6	5.30102999566398	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 1 diabetes	1	1	1	1
rs9653442	5E-6	5.30102999566398	17554260	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs5015480	5E-6	5.30102999566398	17463249	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs10811661	5E-6	5.30102999566398	17463249	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs6013382	5E-6	5.30102999566398	17362836	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.	Amyotrophic lateral sclerosis	1	1	1	1
rs7027203	6E-6	5.22184874961636	23725790	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	DNA methylation (variation)	0	1	1	1
rs12471454	6E-6	5.22184874961636	23728906	A genome-wide association study of sleep habits and insomnia.	Insomnia	1	1	1	1
rs9804200	6E-6	5.22184874961636	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep time	1	1	1	1
rs4073894	6E-6	5.22184874961636	23722424	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.	Educational attainment	1	1	1	1
rs4657482	6E-6	5.22184874961636	23666239	Meta-analysis identifies four new loci associated with testicular germ cell tumor.	Testicular germ cell tumor	0	0	1	1
rs11103429	6E-6	5.22184874961636	23665963	Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease.	Crohn's disease (need for surgery)	1	1	1	1
rs11978472	6E-6	5.22184874961636	23665963	Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease.	Crohn's disease (need for surgery)	1	1	1	1
rs75263140	6E-6	5.22184874961636	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	1	1	1	1
rs2910124	6E-6	5.22184874961636	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs61742849	6E-6	5.22184874961636	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	0	1	1	1
rs74879986	6E-6	5.22184874961636	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs11708304	6E-6	5.22184874961636	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs8024343	6E-6	5.22184874961636	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs142816172	6E-6	5.22184874961636	23568457	Genetic variants associated with disordered eating.	Eating disorders (purging via substances) 	1	1	1	1
rs145433814	6E-6	5.22184874961636	23568457	Genetic variants associated with disordered eating.	Eating disorders (purging via substances) 	NA	NA	NA	NA
rs7187365	6E-6	5.22184874961636	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	1	1	1	1
rs6578985	6E-6	5.22184874961636	23593202	Bivariate genome-wide association analyses identified genes with pleiotropic effects for femoral neck bone geometry and age at menarche.	Femoral neck bone geometry and menarche (age at onset)	0	0	0	0
rs11571833	6E-6	5.22184874961636	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	0	0	1	1
rs12421680	6E-6	5.22184874961636	23548203	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Sunburns	1	1	1	1
rs7577599	6E-6	5.22184874961636	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	0	0	0	0
rs4629710	6E-6	5.22184874961636	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs9504361	6E-6	5.22184874961636	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Pit-and-Fissure caries 	0	1	1	1
rs6806253	6E-6	5.22184874961636	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Pit-and-Fissure caries 	0	1	1	1
rs2078454	6E-6	5.22184874961636	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Smooth-surface caries 	1	1	1	1
rs7816936	6E-6	5.22184874961636	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	1	1	1	1
rs11193561	6E-6	5.22184874961636	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	1	1	1	1
rs10906189	6E-6	5.22184874961636	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	1	1	1	1
rs9375225	6E-6	5.22184874961636	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	0	1	1	1
rs1514174	6E-6	5.22184874961636	23449627	Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.	Pubertal anthropometrics	0	1	1	1
rs1104918	6E-6	5.22184874961636	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs11827962	6E-6	5.22184874961636	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs6889746	6E-6	5.22184874961636	23509613	Genome-wide association study of antiphospholipid antibodies.	Presence of antiphospholipid antibodies	0	1	1	1
rs17791782	6E-6	5.22184874961636	23509613	Genome-wide association study of antiphospholipid antibodies.	Presence of antiphospholipid antibodies	1	1	1	1
rs13403289	6E-6	5.22184874961636	23509613	Genome-wide association study of antiphospholipid antibodies.	Presence of antiphospholipid antibodies	1	1	1	1
rs258401	6E-6	5.22184874961636	23393555	Genome-wide association study of retinopathy in individuals without diabetes.	Retinopathy in non-diabetics	1	1	1	1
rs5763911	6E-6	5.22184874961636	23393555	Genome-wide association study of retinopathy in individuals without diabetes.	Retinopathy in non-diabetics	1	1	1	1
rs4381823	6E-6	5.22184874961636	23894747	A comprehensive family-based replication study of schizophrenia genes.	Schizophrenia	1	1	1	1
rs4585146	6E-6	5.22184874961636	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	0	0	0	0
rs1706631	6E-6	5.22184874961636	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs17634917	6E-6	5.22184874961636	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	0	0	0	0
rs912988	6E-6	5.22184874961636	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs1822818	6E-6	5.22184874961636	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs12210761	6E-6	5.22184874961636	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs6502557	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2189812	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11188352	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4878639	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs16952065	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1672743	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs3097645	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1364477	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs17161553	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2381628	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6494964	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs13072512	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11942476	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs11678036	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10764775	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs16906415	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1054052	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs17835853	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4710520	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6466479	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs17403780	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs8140172	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7532570	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4143912	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs10796849	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs17783561	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2106139	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs12367448	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7649739	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs16844846	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11781525	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs2887004	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10236237	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11880637	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1470506	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11128271	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs17120471	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11675841	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs12664111	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10817408	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10511052	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2110166	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs12127944	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11635553	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7137515	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11847263	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs13148252	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7964407	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1650123	6E-6	5.22184874961636	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1525739	6E-6	5.22184874961636	23386860	Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes.	Type 2 diabetes (dietary heme iron intake interaction)	1	1	1	1
rs6536413	6E-6	5.22184874961636	23358156	Childhood intelligence is heritable, highly polygenic and associated with FNBP1L.	Intelligence (childhood)	1	1	1	1
rs6764388	6E-6	5.22184874961636	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs2843012	6E-6	5.22184874961636	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA)	1	1	1	1
rs4590408	6E-6	5.22184874961636	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA)	1	1	1	1
rs10863681	6E-6	5.22184874961636	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA-5-HIAA Factor score)	1	1	1	1
rs72663955	6E-6	5.22184874961636	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA-5-HIAA Factor score)	1	1	1	1
rs4590408	6E-6	5.22184874961636	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA-5-HIAA Factor score)	0	1	0	0
rs4812466	6E-6	5.22184874961636	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA-5-HIAA Factor score)	1	1	1	1
rs12692432	6E-6	5.22184874961636	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs111426949	6E-6	5.22184874961636	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs12446289	6E-6	5.22184874961636	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs6498068	6E-6	5.22184874961636	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	0	1	1	1
rs62094879	6E-6	5.22184874961636	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs9646096	6E-6	5.22184874961636	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	1	1	1
rs10406174	6E-6	5.22184874961636	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	1	1	1	1
rs1355023	6E-6	5.22184874961636	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	1	1	1
rs17002988	6E-6	5.22184874961636	23703922	A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls.	Uric acid levels	1	1	1	1
rs4760636	6E-6	5.22184874961636	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	1	1	1	1
rs1865075	6E-6	5.22184874961636	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	0	0	0	0
rs605920	6E-6	5.22184874961636	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	1	1	1	1
rs8050136	6E-6	5.22184874961636	23209189	Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21.	Type 2 diabetes	0	0	1	1
rs489332	6E-6	5.22184874961636	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	1	1	1	1
rs4508864	6E-6	5.22184874961636	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	1	1	1
rs13181561	6E-6	5.22184874961636	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	0	1	1	1
rs17832777	6E-6	5.22184874961636	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	1	1	1	1
rs7078219	6E-6	5.22184874961636	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	0	1	1	1
rs9810890	6E-6	5.22184874961636	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs1057510	6E-6	5.22184874961636	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	0	1	1	1
rs1205863	6E-6	5.22184874961636	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs2250402	6E-6	5.22184874961636	22969067	Genetic variants near PDGFRA are associated with corneal curvature in Australians.	Corneal curvature	1	1	1	1
rs12901001	6E-6	5.22184874961636	22961001	Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.	Barrett's esophagus	0	1	1	1
rs7147705	6E-6	5.22184874961636	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis (age of onset)	1	1	1	1
rs11848070	6E-6	5.22184874961636	22881374	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	Alzheimer's disease (late onset)	0	1	1	1
rs1170612	6E-6	5.22184874961636	22885689	Genome-wide association study of multiplex schizophrenia pedigrees.	Schizophrenia	0	1	1	1
rs2726807	6E-6	5.22184874961636	22885689	Genome-wide association study of multiplex schizophrenia pedigrees.	Schizophrenia	1	1	1	1
rs10519201	6E-6	5.22184874961636	22911880	Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits.	Eating disorders	1	1	1	1
rs4848768	6E-6	5.22184874961636	22903471	Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.	Lentiform nucleus volume 	0	0	0	0
rs5951698	6E-6	5.22184874961636	22889924	Genome-wide association study of Tourette's syndrome.	Tourette syndrome	NA	NA	NA	NA
rs6539267	6E-6	5.22184874961636	22889924	Genome-wide association study of Tourette's syndrome.	Tourette syndrome	0	1	1	1
rs769111	6E-6	5.22184874961636	22889924	Genome-wide association study of Tourette's syndrome.	Tourette syndrome	1	1	1	1
rs11097912	6E-6	5.22184874961636	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs10455657	6E-6	5.22184874961636	22823124	The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation.	Cannabis use (initiation)	1	1	1	1
rs293428	6E-6	5.22184874961636	22829776	A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.	Sex hormone-binding globulin levels	0	0	0	0
rs10466033	6E-6	5.22184874961636	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	0	1	1	1
rs1529102	6E-6	5.22184874961636	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	0	1	1	1
rs34479159	6E-6	5.22184874961636	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs7104745	6E-6	5.22184874961636	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	0	1	1	1
rs34065801	6E-6	5.22184874961636	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs61159171	6E-6	5.22184874961636	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs2990510	6E-6	5.22184874961636	22704111	Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.	Erectile dysfunction	0	1	1	1
rs6585436	6E-6	5.22184874961636	22683750	A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern.	Cardiac repolarization	1	1	1	1
rs402675	6E-6	5.22184874961636	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Estradiol levels	1	1	1	1
rs3849491	6E-6	5.22184874961636	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Sex hormone-binding globulin levels	1	1	1	1
rs10495024	6E-6	5.22184874961636	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Testosterone levels	1	1	1	1
rs3104402	6E-6	5.22184874961636	22658931	A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed.	Immune response to anthrax vaccine 	0	1	1	1
rs6478282	6E-6	5.22184874961636	22658931	A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed.	Immune response to anthrax vaccine 	1	1	1	1
rs10172965	6E-6	5.22184874961636	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	1	1	1	1
rs6670533	6E-6	5.22184874961636	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting insulin-related traits (interaction with BMI)	1	1	1	1
rs12583882	6E-6	5.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs11850957	6E-6	5.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs10916025	6E-6	5.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs2059397	6E-6	5.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs9662633	6E-6	5.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	0	1	0	0
rs746080	6E-6	5.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs4821132	6E-6	5.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	0	1	0	0
rs10914967	6E-6	5.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs4978053	6E-6	5.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs10901513	6E-6	5.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs17744121	6E-6	5.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs7085142	6E-6	5.22184874961636	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs1488193	6E-6	5.22184874961636	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs7327064	6E-6	5.22184874961636	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs12713280	6E-6	5.22184874961636	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs10937544	6E-6	5.22184874961636	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	0	0	0	0
rs13325751	6E-6	5.22184874961636	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	1	1	1	1
rs1951681	6E-6	5.22184874961636	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	1	1	1	1
rs9267663	6E-6	5.22184874961636	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	0	1	1	1
rs2226006	6E-6	5.22184874961636	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (fairness)	1	1	1	1
rs7231412	6E-6	5.22184874961636	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	0	0	0	0
rs2904804	6E-6	5.22184874961636	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	1	1	1	1
rs17376026	6E-6	5.22184874961636	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	NA	NA	NA	NA
rs885814	6E-6	5.22184874961636	22569225	Investigation of single nucleotide polymorphisms and biological pathways associated with response to TNFα inhibitors in patients with rheumatoid arthritis.	Response to TNF-alpha inhibitors in rheumatoid arthritis	0	1	1	1
rs9395865	6E-6	5.22184874961636	22554406	Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6.	Electroencephalographic traits in alcoholism	1	1	1	1
rs4658627	6E-6	5.22184874961636	22560479	Genome-wide association study of the age of onset of childhood asthma.	Asthma (childhood onset)	1	1	1	1
rs6456042	6E-6	5.22184874961636	22538805	Genome-wide association identifies the T gene as a novel asthma pharmacogenetic locus.	Asthma	0	1	1	1
rs2173763	6E-6	5.22184874961636	22472876	A mega-analysis of genome-wide association studies for major depressive disorder.	Major depressive disorder	1	1	1	1
rs2675163	6E-6	5.22184874961636	22437554	Genome-wide association study identifies three common variants associated with serologic response to vitamin E supplementation in men.	Response to Vitamin E supplementation	NA	NA	NA	NA
rs933117	6E-6	5.22184874961636	22446040	A novel locus for body mass index on 5p15.2: a meta-analysis of two genome-wide association studies.	Body mass index	0	1	1	1
rs6884431	6E-6	5.22184874961636	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs1867982	6E-6	5.22184874961636	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs9979235	6E-6	5.22184874961636	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs8083432	6E-6	5.22184874961636	22379998	Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.	Adverse response to lamotrigine and phenytoin	1	1	1	1
rs7798500	6E-6	5.22184874961636	22379998	Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.	Adverse response to lamotrigine and phenytoin	1	1	1	1
rs11035577	6E-6	5.22184874961636	22365631	Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.	Temperament (bipolar disorder)	1	1	1	1
rs890835	6E-6	5.22184874961636	22267201	Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.	Menopause (age at onset)	1	1	1	1
rs4234853	6E-6	5.22184874961636	22443383	Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs11613092	6E-6	5.22184874961636	22443383	Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs482329	6E-6	5.22184874961636	22247754	Genome-wide association of implantable cardioverter-defibrillator activation with life-threatening arrhythmias.	Life threatening arrhythmia	1	1	1	1
rs2903698	6E-6	5.22184874961636	22210626	Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.	Prion diseases	0	1	1	1
rs12761224	6E-6	5.22184874961636	22210626	Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.	Prion diseases	1	1	1	1
rs4821544	6E-6	5.22184874961636	22197932	Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis.	Atopic dermatitis	1	1	1	1
rs7738636	6E-6	5.22184874961636	22076464	Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs9375674	6E-6	5.22184874961636	22044751	Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study.	Renal sinus fat 	1	1	1	1
rs1572050	6E-6	5.22184874961636	22044751	Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study.	Renal sinus fat 	1	1	1	1
rs17773430	6E-6	5.22184874961636	22013104	Genome-wide scan for loci of adolescent obesity and their relationship with blood pressure.	Obesity and blood pressure	0	1	1	1
rs4770403	6E-6	5.22184874961636	22004471	Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.	Alcohol dependence	1	1	1	1
rs10137082	6E-6	5.22184874961636	21980299	A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.	Type 1 diabetes	1	1	1	1
rs2647044	6E-6	5.22184874961636	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	0	1	1	1
rs13025591	6E-6	5.22184874961636	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	0	1	1
rs2048672	6E-6	5.22184874961636	21908515	Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium.	Breast cancer	1	1	1	1
rs3739070	6E-6	5.22184874961636	21835309	GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development.	Iris characteristics	0	0	0	0
rs17388568	6E-6	5.22184874961636	21829393	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	Type 1 diabetes autoantibodies	0	0	0	0
rs2298574	6E-6	5.22184874961636	21810271	Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.	vWF and FVIII levels	1	1	1	1
rs4764043	6E-6	5.22184874961636	21782286	A genome-wide association study of aging.	Aging (time to event)	1	1	1	1
rs7315438	6E-6	5.22184874961636	21761138	Meta-analysis of new genome-wide association studies of colorectal cancer risk.	Colorectal cancer	1	1	1	1
rs10858396	6E-6	5.22184874961636	21784300	Genome-wide association study of the child behavior checklist dysregulation profile.	Attention deficit hyperactivity disorder	1	1	1	1
rs742134	6E-6	5.22184874961636	21743057	Genome-wide association study identifies new prostate cancer susceptibility loci.	Prostate cancer	1	1	1	1
rs1412115	6E-6	5.22184874961636	21682944	DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population.	Schizophrenia	1	1	1	1
rs6764363	6E-6	5.22184874961636	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs707040	6E-6	5.22184874961636	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs17149161	6E-6	5.22184874961636	21654844	Genome-wide association study of severity in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs7789940	6E-6	5.22184874961636	21654844	Genome-wide association study of severity in multiple sclerosis.	Multiple sclerosis	0	0	0	0
rs477687	6E-6	5.22184874961636	21502085	Genome-wide association study implicates PARD3B-based AIDS restriction.	AIDS progression	1	1	1	1
rs10253361	6E-6	5.22184874961636	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (alcohol dependence factor score)	1	1	1	1
rs10908907	6E-6	5.22184874961636	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (heaviness of drinking)	1	1	1	1
rs4246856	6E-6	5.22184874961636	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	1	1	1	1
rs8083346	6E-6	5.22184874961636	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	0	1	1	1
rs9378688	6E-6	5.22184874961636	21502949	Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search.	Caudate nucleus volume	1	1	1	1
rs673604	6E-6	5.22184874961636	21499250	Genome-wide association study identifies a common variant associated with risk of endometrial cancer.	Endometrial cancer	1	1	1	1
rs16966142	6E-6	5.22184874961636	21490707	Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.	Caffeine consumption	0	1	1	1
rs10910200	6E-6	5.22184874961636	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs3184504	6E-6	5.22184874961636	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	0	1	1	1
rs2953174	6E-6	5.22184874961636	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	NA	NA	NA	NA
rs1575891	6E-6	5.22184874961636	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	0	1	1	1
rs17259784	6E-6	5.22184874961636	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	1	1	1	1
rs2388436	6E-6	5.22184874961636	21302353	Genome-wide association study of hoarding traits.	Hoarding	1	1	1	1
rs12024204	6E-6	5.22184874961636	21151130	Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis.	Endometriosis	1	1	1	1
rs2839627	6E-6	5.22184874961636	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	0	1	1	1
rs903027	6E-6	5.22184874961636	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	MRI atrophy measures	1	1	1	1
rs10494067	6E-6	5.22184874961636	21079607	A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.	Anorexia nervosa	1	1	1	1
rs2383378	6E-6	5.22184874961636	21079607	A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.	Anorexia nervosa	1	1	1	1
rs1795648	6E-6	5.22184874961636	21057379	Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes.	Bipolar disorder and schizophrenia	1	1	1	1
rs12457996	6E-6	5.22184874961636	21042317	Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned.	Major depressive disorder	0	1	1	1
rs7602460	6E-6	5.22184874961636	21041692	Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science.	Atrioventricular conduction	1	1	1	1
rs12032381	6E-6	5.22184874961636	20971583	Genome-wide association scan of Dupuytren's disease.	Dupuytren's disease	1	1	1	1
rs842636	6E-6	5.22184874961636	20953189	Genome-wide association analysis identifies three psoriasis susceptibility loci.	Psoriasis	0	0	1	1
rs7081678	6E-6	5.22184874961636	20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Waist-hip ratio	1	1	1	1
rs7735699	6E-6	5.22184874961636	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs10486158	6E-6	5.22184874961636	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs11258317	6E-6	5.22184874961636	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs11955175	6E-6	5.22184874961636	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs13183791	6E-6	5.22184874961636	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1446682	6E-6	5.22184874961636	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1704734	6E-6	5.22184874961636	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs213443	6E-6	5.22184874961636	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	NA	NA	NA	NA
rs2643217	6E-6	5.22184874961636	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs767770	6E-6	5.22184874961636	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs17864092	6E-6	5.22184874961636	20800221	Genome-wide association scan of trait depression.	Depression (quantitative trait)	1	1	1	1
rs2999399	6E-6	5.22184874961636	20709820	Genome-wide association study identifies BICD1 as a susceptibility gene for emphysema.	Emphysema-related traits	1	1	1	1
rs7911712	6E-6	5.22184874961636	20709820	Genome-wide association study identifies BICD1 as a susceptibility gene for emphysema.	Emphysema-related traits	1	1	1	1
rs1780159	6E-6	5.22184874961636	20705733	Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.	Calcium levels	1	1	1	1
rs6091737	6E-6	5.22184874961636	20705733	Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.	Calcium levels	1	1	1	1
rs6027755	6E-6	5.22184874961636	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs2234978	6E-6	5.22184874961636	20694011	Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.	Immunoglobulin A 	1	1	1	1
rs9810857	6E-6	5.22184874961636	20732626	Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	1	1	1	1
rs3184504	6E-6	5.22184874961636	20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Rheumatoid arthritis	0	1	1	1
rs1523288	6E-6	5.22184874961636	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	1	1	1	1
rs11880198	6E-6	5.22184874961636	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	1	1	1	1
rs7260329	6E-6	5.22184874961636	20418888	Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior.	Smoking behavior	1	1	1	1
rs10858945	6E-6	5.22184874961636	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (cup)	1	1	1	1
rs10123041	6E-6	5.22184874961636	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs2901331	6E-6	5.22184874961636	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs10221833	6E-6	5.22184874961636	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	0	1	1	1
rs2352028	6E-6	5.22184874961636	20304703	Genetic variants and risk of lung cancer in never smokers: a genome-wide association study.	Lung cancer	1	1	1	1
rs6501384	6E-6	5.22184874961636	20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Eosinophilic esophagitis (pediatric)	0	1	1	1
rs13278732	6E-6	5.22184874961636	20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Eosinophilic esophagitis (pediatric)	1	1	1	1
rs2506933	6E-6	5.22184874961636	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs6574433	6E-6	5.22184874961636	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	0	1	1	1
rs3784962	6E-6	5.22184874961636	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	0	0	0	0
rs6017291	6E-6	5.22184874961636	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs34704616	6E-6	5.22184874961636	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs17144465	6E-6	5.22184874961636	20125088	Genome-wide association study of recurrent early-onset major depressive disorder.	Major depressive disorder	0	1	1	1
rs12049330	6E-6	5.22184874961636	20125088	Genome-wide association study of recurrent early-onset major depressive disorder.	Major depressive disorder	0	0	0	0
rs5990417	6E-6	5.22184874961636	20038947	Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.	Major depressive disorder (broad)	NA	NA	NA	NA
rs2069084	6E-6	5.22184874961636	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs1405262	6E-6	5.22184874961636	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs8017455	6E-6	5.22184874961636	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	0	1	1	1
rs1024889	6E-6	5.22184874961636	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Body mass index	1	1	1	1
rs1927702	6E-6	5.22184874961636	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Body mass index	0	1	1	1
rs12517906	6E-6	5.22184874961636	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Body mass index	0	1	0	0
rs1152846	6E-6	5.22184874961636	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Weight	0	1	0	0
rs2765086	6E-6	5.22184874961636	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Weight	1	1	1	1
rs11064994	6E-6	5.22184874961636	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs9442235	6E-6	5.22184874961636	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs12639834	6E-6	5.22184874961636	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs3772130	6E-6	5.22184874961636	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	0	1	1	1
rs960089	6E-6	5.22184874961636	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs1078373	6E-6	5.22184874961636	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs11984145	6E-6	5.22184874961636	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs9290663	6E-6	5.22184874961636	19684603	Germline genomic variants associated with childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	0	1	1	1
rs4845552	6E-6	5.22184874961636	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs6031882	6E-6	5.22184874961636	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	0	0	0	0
rs2274459	6E-6	5.22184874961636	19553259	Common body mass index-associated variants confer risk of extreme obesity.	Obesity (extreme)	0	0	0	0
rs4680534	6E-6	5.22184874961636	19525953	Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.	Multiple sclerosis	0	1	1	1
rs6990255	6E-6	5.22184874961636	19416921	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.	Bipolar disorder	0	1	1	1
rs2905072	6E-6	5.22184874961636	19416921	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.	Bipolar disorder	1	1	1	1
rs10411195	6E-6	5.22184874961636	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	1	1	1	1
rs7050529	6E-6	5.22184874961636	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	NA	NA	NA	NA
rs11082304	6E-6	5.22184874961636	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	0	1	1	1
rs933688	6E-6	5.22184874961636	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	1	1	1	1
rs1889899	6E-6	5.22184874961636	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	0	1	1	1
rs10989661	6E-6	5.22184874961636	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	1	1	1	1
rs3112740	6E-6	5.22184874961636	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	1	1	1	1
rs7590983	6E-6	5.22184874961636	19260139	Genome-wide association study of anthropometric traits in Korcula Island, Croatia.	Anthropometric traits	1	1	1	1
rs7792939	6E-6	5.22184874961636	19260139	Genome-wide association study of anthropometric traits in Korcula Island, Croatia.	Anthropometric traits	0	0	0	0
rs157350	6E-6	5.22184874961636	19260139	Genome-wide association study of anthropometric traits in Korcula Island, Croatia.	Anthropometric traits	0	0	0	0
rs201789	6E-6	5.22184874961636	19260139	Genome-wide association study of anthropometric traits in Korcula Island, Croatia.	Anthropometric traits	0	1	1	1
rs10444502	6E-6	5.22184874961636	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	0	0	0	0
rs10516430	6E-6	5.22184874961636	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	1	1	1	1
rs1076160	6E-6	5.22184874961636	19169254	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.	Psoriasis	0	1	1	1
rs4238010	6E-6	5.22184874961636	19107115	Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts.	Major depressive disorder	1	1	1	1
rs4820268	6E-6	5.22184874961636	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	0	1	1
rs1006899	6E-6	5.22184874961636	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (spine)	1	1	1	1
rs2145270	6E-6	5.22184874961636	19079261	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.	Body mass index	0	0	1	1
rs930421	6E-6	5.22184874961636	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	0	1	0	0
rs17651978	6E-6	5.22184874961636	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	1	1	1	1
rs4147141	6E-6	5.22184874961636	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	0	1	0	0
rs3892715	6E-6	5.22184874961636	18937294	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.	Attention deficit hyperactivity disorder (time to onset)	1	1	1	1
rs6610953	6E-6	5.22184874961636	18957941	Genome-wide association scan for five major dimensions of personality.	Personality dimensions	NA	NA	NA	NA
rs2088885	6E-6	5.22184874961636	19023125	A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype.	Brain imaging in schizophrenia (interaction)	1	1	1	1
rs2039485	6E-6	5.22184874961636	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Brain lesion load	1	1	1	1
rs12047808	6E-6	5.22184874961636	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (age of onset)	1	1	1	1
rs6941421	6E-6	5.22184874961636	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (severity)	1	1	1	1
rs7191888	6E-6	5.22184874961636	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (severity)	1	1	1	1
rs180358	6E-6	5.22184874961636	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (severity)	0	1	1	1
rs10243024	6E-6	5.22184874961636	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (severity)	1	1	1	1
rs3826656	6E-6	5.22184874961636	18976728	Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE.	Alzheimer's disease	0	1	1	1
rs10815798	6E-6	5.22184874961636	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	0	1	1	1
rs1381102	6E-6	5.22184874961636	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs7236632	6E-6	5.22184874961636	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs412050	6E-6	5.22184874961636	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	0	1	1	1
rs332034	6E-6	5.22184874961636	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	1	1	1	1
rs9990174	6E-6	5.22184874961636	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	1	1	1	1
rs2395528	6E-6	5.22184874961636	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	1	1	1	1
rs6085920	6E-6	5.22184874961636	18759275	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish.	Uric acid levels	1	1	1	1
rs2705293	6E-6	5.22184874961636	18762592	Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism.	Neuroticism	0	1	1	1
rs1948368	6E-6	5.22184874961636	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	1	1	1	1
rs7042161	6E-6	5.22184874961636	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	1	1	1	1
rs544368	6E-6	5.22184874961636	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	1	1	1	1
rs2278702	6E-6	5.22184874961636	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	1	1	1	1
rs2002842	6E-6	5.22184874961636	18668548	Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility.	Rheumatoid arthritis	1	1	1	1
rs7192086	6E-6	5.22184874961636	18677311	Identification of loci associated with schizophrenia by genome-wide association and follow-up.	Schizophrenia	1	1	1	1
rs12093699	6E-6	5.22184874961636	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	1	1	1
rs11683229	6E-6	5.22184874961636	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	1	1	1
rs10092658	6E-6	5.22184874961636	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs7076247	6E-6	5.22184874961636	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	1	1	1
rs1207421	6E-6	5.22184874961636	18471798	Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis.	Knee osteoarthritis	1	1	1	1
rs6899976	6E-6	5.22184874961636	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs5751614	6E-6	5.22184874961636	18391951	Many sequence variants affecting diversity of adult human height.	Height	1	1	1	1
rs17083844	6E-6	5.22184874961636	18204098	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.	Systemic lupus erythematosus	1	1	1	1
rs10514688	6E-6	5.22184874961636	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Tonometry	1	1	1	1
rs7042864	6E-6	5.22184874961636	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Tonometry	0	1	1	1
rs291353	6E-6	5.22184874961636	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Aging traits	1	1	1	1
rs180730	6E-6	5.22184874961636	17903298	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	Fasting plasma glucose	0	0	0	0
rs458685	6E-6	5.22184874961636	17903305	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	Breast cancer	0	1	1	1
rs1876206	6E-6	5.22184874961636	17903305	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	Breast cancer	0	1	1	1
rs10483853	6E-6	5.22184874961636	17903303	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	Coronary artery calcification	0	1	1	1
rs1400544	6E-6	5.22184874961636	17903303	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	Subclinical atherosclerosis traits (other)	1	1	1	1
rs7715811	6E-6	5.22184874961636	17903303	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	Subclinical atherosclerosis traits (other)	0	0	0	0
rs1031381	6E-6	5.22184874961636	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Cognitive test performance	1	1	1	1
rs10489896	6E-6	5.22184874961636	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Cognitive test performance	1	1	1	1
rs952700	6E-6	5.22184874961636	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Volumetric brain MRI	1	1	1	1
rs1935881	6E-6	5.22184874961636	17903301	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	Echocardiographic traits	1	1	1	1
rs10498091	6E-6	5.22184874961636	17903301	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	Echocardiographic traits	1	1	1	1
rs2553268	6E-6	5.22184874961636	17903301	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	Exercise treadmill test traits	1	1	1	1
rs730532	6E-6	5.22184874961636	17903307	Framingham Heart Study genome-wide association: results for pulmonary function measures.	Pulmonary function	1	1	1	1
rs2357013	6E-6	5.22184874961636	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	0	0	0	0
rs1829883	6E-6	5.22184874961636	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs1200821	6E-6	5.22184874961636	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	0	1	1	1
rs10484128	6E-6	5.22184874961636	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	0	1	1	1
rs636864	6E-6	5.22184874961636	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	0	1	1	1
rs6108011	6E-6	5.22184874961636	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs6712932	6E-6	5.22184874961636	17668382	Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium.	Type 2 diabetes	1	1	1	1
rs8055236	6E-6	5.22184874961636	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Coronary heart disease	1	1	1	1
rs2398162	6E-6	5.22184874961636	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Hypertension	0	1	1	1
rs10486776	6E-6	5.22184874961636	17434096	A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.	Stroke	1	1	1	1
rs9536591	6E-6	5.22184874961636	17434096	A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.	Stroke	1	1	1	1
rs2782931	6E-6	5.22184874961636	17362836	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.	Amyotrophic lateral sclerosis	1	1	1	1
rs12913538	7E-6	5.15490195998574	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep depth	1	1	1	1
rs13068101	7E-6	5.15490195998574	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep time	1	1	1	1
rs12640626	7E-6	5.15490195998574	23722424	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.	Educational attainment	0	1	1	1
rs997154	7E-6	5.15490195998574	23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Primary tooth development (time to first tooth eruption)	0	1	0	0
rs2029213	7E-6	5.15490195998574	23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Heart rate	0	1	1	1
rs8050187	7E-6	5.15490195998574	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	1	1	1	1
rs17496827	7E-6	5.15490195998574	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	1	1	1	1
rs7724774	7E-6	5.15490195998574	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs78661745	7E-6	5.15490195998574	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	0	1	1	1
rs10776614	7E-6	5.15490195998574	23593239	The molecular genetic architecture of self-employment.	Self-employment	1	1	1	1
rs1432679	7E-6	5.15490195998574	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	0	0	1	1
rs11259403	7E-6	5.15490195998574	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (asthmatics)	1	1	1	1
rs3780215	7E-6	5.15490195998574	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (asthmatics)	1	1	1	1
rs2665390	7E-6	5.15490195998574	23544013	Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.	Ovarian cancer in BRCA1 mutation carriers 	0	1	1	1
rs8028689	7E-6	5.15490195998574	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	0	1	1	1
rs12545912	7E-6	5.15490195998574	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (hyperdiploidy)	0	0	0	0
rs3825807	7E-6	5.15490195998574	23561647	Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction.	Coronary artery calcification	0	1	1	1
rs2022068	7E-6	5.15490195998574	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Pit-and-Fissure caries 	1	1	1	1
rs10486722	7E-6	5.15490195998574	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Pit-and-Fissure caries 	1	1	1	1
rs10431397	7E-6	5.15490195998574	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	1	1	1	1
rs8058295	7E-6	5.15490195998574	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs7254215	7E-6	5.15490195998574	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs7069733	7E-6	5.15490195998574	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs4741652	7E-6	5.15490195998574	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs159788	7E-6	5.15490195998574	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs7565792	7E-6	5.15490195998574	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs11587682	7E-6	5.15490195998574	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs6681460	7E-6	5.15490195998574	23509613	Genome-wide association study of antiphospholipid antibodies.	Presence of antiphospholipid antibodies	0	1	1	1
rs12204683	7E-6	5.15490195998574	23509613	Genome-wide association study of antiphospholipid antibodies.	Presence of antiphospholipid antibodies	1	1	1	1
rs9315762	7E-6	5.15490195998574	23509613	Genome-wide association study of antiphospholipid antibodies.	Presence of antiphospholipid antibodies	1	1	1	1
rs6080100	7E-6	5.15490195998574	23509613	Genome-wide association study of antiphospholipid antibodies.	Presence of antiphospholipid antibodies	1	1	1	1
rs1821625	7E-6	5.15490195998574	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs4916321	7E-6	5.15490195998574	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs12500612	7E-6	5.15490195998574	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs6534441	7E-6	5.15490195998574	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs11149178	7E-6	5.15490195998574	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs604222	7E-6	5.15490195998574	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs9563960	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs909814	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs7691216	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7978454	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs1550584	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11255400	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1386809	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2919024	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2126200	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs2504183	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs909848	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6064045	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7101378	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs2841233	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7734156	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9394438	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs17666538	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs3845441	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1904173	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs17558301	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2614463	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2744203	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4076555	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10817408	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs17153352	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6928844	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1001579	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs10813957	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1547201	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4143912	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1673866	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7194356	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9492645	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1339738	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6421315	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs38989	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2530545	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6466479	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs16949825	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11212260	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2844479	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1122979	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2270788	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs3097645	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10236237	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs12455580	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6583437	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs435066	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs17403780	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10751776	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs3213473	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6059594	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10113903	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11706018	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs738144	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs12213468	7E-6	5.15490195998574	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6042314	7E-6	5.15490195998574	23358156	Childhood intelligence is heritable, highly polygenic and associated with FNBP1L.	Intelligence (childhood)	1	1	1	1
rs17312292	7E-6	5.15490195998574	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs12593811	7E-6	5.15490195998574	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs2244067	7E-6	5.15490195998574	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA)	1	1	1	1
rs6559140	7E-6	5.15490195998574	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA)	1	1	1	1
rs279612	7E-6	5.15490195998574	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA)	1	1	1	1
rs73114594	7E-6	5.15490195998574	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA/ MHPG Ratio)	1	1	1	1
rs5910235	7E-6	5.15490195998574	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA/ MHPG Ratio)	NA	NA	NA	NA
rs9460635	7E-6	5.15490195998574	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA-5-HIAA Factor score)	0	1	1	1
rs71327718	7E-6	5.15490195998574	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/5-HIAA ratio)	1	1	1	1
rs73628692	7E-6	5.15490195998574	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/5-HIAA ratio)	1	1	1	1
rs13012266	7E-6	5.15490195998574	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	0	1	1	1
rs184891496	7E-6	5.15490195998574	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs2039964	7E-6	5.15490195998574	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs6721654	7E-6	5.15490195998574	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	0	0	0
rs7750345	7E-6	5.15490195998574	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	0	0	0
rs10406174	7E-6	5.15490195998574	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	0	0	0
rs4813802	7E-6	5.15490195998574	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	1	1	1	1
rs4438497	7E-6	5.15490195998574	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs6973392	7E-6	5.15490195998574	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs2888830	7E-6	5.15490195998574	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	0	0	0	0
rs899967	7E-6	5.15490195998574	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	1	1	1	1
rs1351267	7E-6	5.15490195998574	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	0	1	1	1
rs10924245	7E-6	5.15490195998574	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	1	1	1	1
rs9390123	7E-6	5.15490195998574	23108145	Genome-wide association study reveals novel genetic determinants of DNA repair capacity in lung cancer.	Lung Cancer (DNA repair capacity)	1	1	1	1
rs1680005	7E-6	5.15490195998574	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	1	1	1	1
rs12617721	7E-6	5.15490195998574	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	0	1	1	1
rs17485138	7E-6	5.15490195998574	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	1	1	1	1
rs12038826	7E-6	5.15490195998574	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs11918654	7E-6	5.15490195998574	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs11987235	7E-6	5.15490195998574	22969067	Genetic variants near PDGFRA are associated with corneal curvature in Australians.	Corneal curvature	0	1	1	1
rs2693676	7E-6	5.15490195998574	22969067	Genetic variants near PDGFRA are associated with corneal curvature in Australians.	Corneal curvature	1	1	1	1
rs7607369	7E-6	5.15490195998574	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	0	0	0	0
rs1320900	7E-6	5.15490195998574	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	1	1	1	1
rs6918777	7E-6	5.15490195998574	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	1	1	1	1
rs7047865	7E-6	5.15490195998574	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis (age of onset)	0	1	1	1
rs4937314	7E-6	5.15490195998574	22881374	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	Alzheimer's disease (late onset)	1	1	1	1
rs16934812	7E-6	5.15490195998574	22885689	Genome-wide association study of multiplex schizophrenia pedigrees.	Schizophrenia	1	1	1	1
rs1869839	7E-6	5.15490195998574	22936669	A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.	Crohn's disease	1	1	1	1
rs9995093	7E-6	5.15490195998574	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	1	1	1	1
rs4467006	7E-6	5.15490195998574	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	0	0	0	0
rs7690467	7E-6	5.15490195998574	22911880	Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits.	Eating disorders	1	1	1	1
rs218361	7E-6	5.15490195998574	22911880	Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits.	Eating disorders	1	1	1	1
rs10952132	7E-6	5.15490195998574	22890011	Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate.	Response to fenofibrate	0	0	0	0
rs7846606	7E-6	5.15490195998574	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs3815854	7E-6	5.15490195998574	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs17086172	7E-6	5.15490195998574	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs9458975	7E-6	5.15490195998574	22823124	The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation.	Cannabis use (initiation)	NA	NA	NA	NA
rs11875185	7E-6	5.15490195998574	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	1	1	1	1
rs158856	7E-6	5.15490195998574	22754043	A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.	Insomnia (caffeine-induced)	1	1	1	1
rs2716816	7E-6	5.15490195998574	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs4262150	7E-6	5.15490195998574	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs10795130	7E-6	5.15490195998574	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Sex hormone-binding globulin levels	1	1	1	1
rs10263087	7E-6	5.15490195998574	22648509	PKNOX2 is associated with formal thought disorder in schizophrenia: a meta-analysis of two genome-wide association studies.	Formal thought disorder in schizophrenia	1	1	1	1
rs11018023	7E-6	5.15490195998574	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	1	1	1	1
rs10811661	7E-6	5.15490195998574	22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Fasting glucose-related traits (interaction with BMI)	0	1	1	1
rs12773846	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs11952171	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs2058059	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs12967884	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs12467609	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	0	1	1	1
rs7602441	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs2554152	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs17302400	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs10961577	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs13043330	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	0	1	1	1
rs1048497	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	0	0	0
rs16912285	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs12486865	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs745978	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs11161851	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs11998649	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs10066447	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs10176755	7E-6	5.15490195998574	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs438895	7E-6	5.15490195998574	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs1399090	7E-6	5.15490195998574	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs1570854	7E-6	5.15490195998574	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (environmentalism)	1	1	1	1
rs117294	7E-6	5.15490195998574	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (fairness)	1	1	1	1
rs16854884	7E-6	5.15490195998574	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (feminism/equality)	1	1	1	1
rs10754644	7E-6	5.15490195998574	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (feminism/equality)	1	1	1	1
rs10146615	7E-6	5.15490195998574	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	1	1	1	1
rs138597	7E-6	5.15490195998574	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (time)	1	1	1	1
rs10897449	7E-6	5.15490195998574	22554406	Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6.	Electroencephalographic traits in alcoholism	1	1	1	1
rs1386478	7E-6	5.15490195998574	22482804	Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.	Crohn's disease and psoriasis	1	1	1	1
rs10961534	7E-6	5.15490195998574	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	1	1	1	1
rs9901756	7E-6	5.15490195998574	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	1	1	1	1
rs10248351	7E-6	5.15490195998574	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	1	1	1	1
rs10519980	7E-6	5.15490195998574	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	0	1	1	1
rs655167	7E-6	5.15490195998574	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	1	1	1	1
rs231779	7E-6	5.15490195998574	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	0	1	1	1
rs1476587	7E-6	5.15490195998574	22479309	Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts.	Brachial circumference	0	1	1	1
rs11023332	7E-6	5.15490195998574	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	1	1	1
rs2278170	7E-6	5.15490195998574	22470424	A high-density genome-wide association screen of sporadic ALS in US veterans.	Amyotrophic lateral sclerosis	1	1	1	1
rs4752485	7E-6	5.15490195998574	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs12436689	7E-6	5.15490195998574	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	0	1	1	1
rs17121403	7E-6	5.15490195998574	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs12712969	7E-6	5.15490195998574	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	NA	NA	NA	NA
rs180273	7E-6	5.15490195998574	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	0	1	1	1
rs1148186	7E-6	5.15490195998574	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs6987004	7E-6	5.15490195998574	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs11615916	7E-6	5.15490195998574	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs12941150	7E-6	5.15490195998574	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs17002253	7E-6	5.15490195998574	22379998	Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.	Adverse response to lamotrigine and phenytoin	1	1	1	1
rs12125971	7E-6	5.15490195998574	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	0	1	1	1
rs17458018	7E-6	5.15490195998574	22319020	A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.	Coronary heart disease	1	1	1	1
rs27524	7E-6	5.15490195998574	22286212	Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups.	Hodgkin's lymphoma	0	1	1	1
rs9806762	7E-6	5.15490195998574	22388998	Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation.	Gaucher disease severity	1	1	1	1
rs1959947	7E-6	5.15490195998574	22443383	Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.	Hemostatic factors and hematological phenotypes	0	1	1	1
rs730129	7E-6	5.15490195998574	22443383	Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.	Hemostatic factors and hematological phenotypes	1	1	1	1
rs17763373	7E-6	5.15490195998574	22210626	Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.	Prion diseases	1	1	1	1
rs730566	7E-6	5.15490195998574	22210626	Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.	Prion diseases	0	1	1	1
rs10108954	7E-6	5.15490195998574	22210626	Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.	Prion diseases	1	1	1	1
rs2137111	7E-6	5.15490195998574	22216198	A genome-wide association study of the Protein C anticoagulant pathway.	Anticoagulant levels	0	1	1	1
rs4659996	7E-6	5.15490195998574	22199011	Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.	Ankle-brachial index 	1	1	1	1
rs7512221	7E-6	5.15490195998574	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	0	1	1	1
rs10078	7E-6	5.15490195998574	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	0	1	1	1
rs12144715	7E-6	5.15490195998574	22095909	Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.	Response to hepatitis C treatment	1	1	1	1
rs12527818	7E-6	5.15490195998574	22095909	Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.	Response to hepatitis C treatment	1	1	1	1
rs9805786	7E-6	5.15490195998574	22064162	Genome-wide association study of comorbid depressive syndrome and alcohol dependence.	Depression and alcohol dependence	1	1	1	1
rs17736767	7E-6	5.15490195998574	22044751	Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study.	Renal sinus fat 	1	1	1	1
rs2556378	7E-6	5.15490195998574	22012869	Genome-wide association study in German patients with attention deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	1	1	1	1
rs2104362	7E-6	5.15490195998574	22005931	Genome-wide association analysis of age-at-onset in Alzheimer's disease.	Alzheimer's disease (age of onset)	1	1	1	1
rs9594293	7E-6	5.15490195998574	21993531	Genome-wide association study does not reveal major genetic determinants for anti-cytomegalovirus antibody response.	Cytomegalovirus antibody response	1	1	1	1
rs1879248	7E-6	5.15490195998574	21926974	Genome-wide association study identifies five new schizophrenia loci.	Schizophrenia	0	0	1	1
rs4332037	7E-6	5.15490195998574	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	0	1	1	1
rs381815	7E-6	5.15490195998574	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	0	0	0
rs2243123	7E-6	5.15490195998574	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs1757948	7E-6	5.15490195998574	21810271	Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.	vWF and FVIII levels	1	1	1	1
rs3112530	7E-6	5.15490195998574	21782286	A genome-wide association study of aging.	Aging (time to event)	1	1	1	1
rs11778329	7E-6	5.15490195998574	21784300	Genome-wide association study of the child behavior checklist dysregulation profile.	Attention deficit hyperactivity disorder	1	1	1	1
rs5762311	7E-6	5.15490195998574	21658281	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	Sudden cardiac arrest	1	1	1	1
rs6785504	7E-6	5.15490195998574	21659360	Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial.	Response to antineoplastic agents	0	0	0	0
rs11645366	7E-6	5.15490195998574	21602797	Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.	Cystic fibrosis severity	1	1	1	1
rs925642	7E-6	5.15490195998574	21552555	A genome-wide association study on obesity and obesity-related traits.	Obesity	1	1	1	1
rs237238	7E-6	5.15490195998574	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (12-month weekly alcohol consumption)	1	1	1	1
rs933769	7E-6	5.15490195998574	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (alcohol dependence factor score)	1	1	1	1
rs4293630	7E-6	5.15490195998574	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (alcohol dependence factor score)	1	1	1	1
rs687621	7E-6	5.15490195998574	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	0	1	1	1
rs7447447	7E-6	5.15490195998574	21490707	Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.	Caffeine consumption	1	1	1	1
rs11765845	7E-6	5.15490195998574	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs11867934	7E-6	5.15490195998574	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	0	1	1	1
rs10411161	7E-6	5.15490195998574	21424380	Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibility.	Breast cancer	1	1	1	1
rs10933436	7E-6	5.15490195998574	21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Coronary heart disease	1	1	1	1
rs10737562	7E-6	5.15490195998574	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	1	1	1	1
rs7927370	7E-6	5.15490195998574	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	1	1	1	1
rs10129255	7E-6	5.15490195998574	21326860	Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study.	Kawasaki disease	1	1	1	1
rs1568657	7E-6	5.15490195998574	21326860	Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study.	Kawasaki disease	1	1	1	1
rs2609653	7E-6	5.15490195998574	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	0	0	1	1
rs6009824	7E-6	5.15490195998574	21273288	Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster.	Natriuretic peptide levels	1	1	1	1
rs975121	7E-6	5.15490195998574	21139019	A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum.	Ileal carcinoids	1	1	1	1
rs7566934	7E-6	5.15490195998574	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs2908835	7E-6	5.15490195998574	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs6961611	7E-6	5.15490195998574	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs7179456	7E-6	5.15490195998574	21182207	Variants in several genomic regions associated with asperger disorder.	Asperger disorder	1	1	1	1
rs17581368	7E-6	5.15490195998574	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Entorhinal cortical thickness	1	1	1	1
rs732528	7E-6	5.15490195998574	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Entorhinal cortical thickness	1	1	1	1
rs11618202	7E-6	5.15490195998574	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	MRI atrophy measures	NA	NA	NA	NA
rs6686643	7E-6	5.15490195998574	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	1	1	1	1
rs9574199	7E-6	5.15490195998574	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	1	1	1	1
rs4318070	7E-6	5.15490195998574	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	0	1	1	1
rs410644	7E-6	5.15490195998574	21079607	A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.	Anorexia nervosa	1	1	1	1
rs11708996	7E-6	5.15490195998574	21076409	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Ventricular conduction	0	1	1	1
rs4571457	7E-6	5.15490195998574	20848476	Genetic predictors of medically refractory ulcerative colitis.	Ulcerative colitis	0	1	1	1
rs17323670	7E-6	5.15490195998574	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs6607284	7E-6	5.15490195998574	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs2398668	7E-6	5.15490195998574	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	0	0	0
rs2424635	7E-6	5.15490195998574	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs10815468	7E-6	5.15490195998574	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs134882	7E-6	5.15490195998574	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs173896	7E-6	5.15490195998574	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs2276498	7E-6	5.15490195998574	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs2530215	7E-6	5.15490195998574	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs913246	7E-6	5.15490195998574	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs11143230	7E-6	5.15490195998574	20877300	Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project.	Suicidal ideation	0	0	0	0
rs2738459	7E-6	5.15490195998574	20864672	Genetic variants influencing circulating lipid levels and risk of coronary artery disease.	LDL cholesterol	1	1	1	1
rs13117816	7E-6	5.15490195998574	20802204	Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis.	Multiple sclerosis--Brain Glutamate Levels	1	1	1	1
rs1449984	7E-6	5.15490195998574	20800221	Genome-wide association scan of trait depression.	Depression (quantitative trait)	1	1	1	1
rs780093	7E-6	5.15490195998574	20705733	Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.	Calcium levels	0	1	1	1
rs13195786	7E-6	5.15490195998574	20705733	Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.	Calcium levels	1	1	1	1
rs10954668	7E-6	5.15490195998574	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (lobular)	0	1	1	1
rs7077164	7E-6	5.15490195998574	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (lobular)	0	0	0	0
rs6079395	7E-6	5.15490195998574	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	0	1	1	1
rs10510146	7E-6	5.15490195998574	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	NA	NA	NA	NA
rs959903	7E-6	5.15490195998574	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs961831	7E-6	5.15490195998574	20691247	A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality.	Personality dimensions	1	1	1	1
rs1533665	7E-6	5.15490195998574	20691247	A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality.	Personality dimensions	1	1	1	1
rs1027730	7E-6	5.15490195998574	20732625	Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	1	1	1	1
rs12680109	7E-6	5.15490195998574	20732625	Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	1	1	1	1
rs10520045	7E-6	5.15490195998574	20673876	Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression.	Major depressive disorder	1	1	1	1
rs1391511	7E-6	5.15490195998574	20662065	Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus.	Neonatal lupus	1	1	1	1
rs6457327	7E-6	5.15490195998574	20639881	Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.	Follicular lymphoma	0	0	1	1
rs179429	7E-6	5.15490195998574	20526338	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Platelet aggregation	1	1	1	1
rs310501	7E-6	5.15490195998574	20516156	Genome-wide association study of major recurrent depression in the U.K. population.	Major depressive disorder	1	1	1	1
rs11118620	7E-6	5.15490195998574	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	0	1	1	1
rs13225783	7E-6	5.15490195998574	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	1	1	1	1
rs7120489	7E-6	5.15490195998574	20400778	Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.	Mortality among heart failure patients	1	1	1	1
rs4979906	7E-6	5.15490195998574	20400778	Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.	Mortality among heart failure patients	1	1	1	1
rs8017423	7E-6	5.15490195998574	20400778	Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.	Mortality among heart failure patients	0	1	1	1
rs1436900	7E-6	5.15490195998574	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (cup)	1	1	1	1
rs12741973	7E-6	5.15490195998574	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (rim)	0	1	1	1
rs1776897	7E-6	5.15490195998574	20397748	Genome-wide association study of height and body mass index in Australian twin families.	Height	0	0	1	1
rs10950821	7E-6	5.15490195998574	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs1535	7E-6	5.15490195998574	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	0	0	0	0
rs2954038	7E-6	5.15490195998574	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	0	1	1	1
rs7236477	7E-6	5.15490195998574	20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Eosinophilic esophagitis (pediatric)	1	1	1	1
rs11989782	7E-6	5.15490195998574	20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Eosinophilic esophagitis (pediatric)	1	1	1	1
rs9804317	7E-6	5.15490195998574	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	0	1	1	1
rs17638629	7E-6	5.15490195998574	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs6118083	7E-6	5.15490195998574	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs2326810	7E-6	5.15490195998574	20038947	Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.	Major depressive disorder (broad)	1	1	1	1
rs1612122	7E-6	5.15490195998574	20038947	Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.	Major depressive disorder (broad)	0	1	1	1
rs16936455	7E-6	5.15490195998574	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs12012519	7E-6	5.15490195998574	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	NA	NA	NA	NA
rs11143609	7E-6	5.15490195998574	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs1120787	7E-6	5.15490195998574	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs2304069	7E-6	5.15490195998574	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs17760296	7E-6	5.15490195998574	20023658	Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.	Orofacial clefts	1	1	1	1
rs10781500	7E-6	5.15490195998574	19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Ulcerative colitis	0	0	1	1
rs6544997	7E-6	5.15490195998574	19890347	Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8.	Vitiligo	1	1	1	1
rs1458095	7E-6	5.15490195998574	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Body mass index	0	1	1	1
rs4751178	7E-6	5.15490195998574	19786962	First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children.	Speech perception in dyslexia	1	1	1	1
rs1020064	7E-6	5.15490195998574	19754311	Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03).	AIDS	1	1	1	1
rs904251	7E-6	5.15490195998574	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs3781684	7E-6	5.15490195998574	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs12423712	7E-6	5.15490195998574	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs1757171	7E-6	5.15490195998574	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	0	0	0	0
rs8097348	7E-6	5.15490195998574	19727025	Genome-wide association study of exercise behavior in Dutch and American adults.	Exercise (leisure time)	1	1	1	1
rs9400317	7E-6	5.15490195998574	19684573	Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance.	Response to hepatitis C treatment	0	1	1	1
rs6428370	7E-6	5.15490195998574	19684603	Germline genomic variants associated with childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	0	1	1	1
rs1881797	7E-6	5.15490195998574	19684603	Germline genomic variants associated with childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	0	1	1	1
rs337847	7E-6	5.15490195998574	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs13160562	7E-6	5.15490195998574	19581569	Genome-wide association study of alcohol dependence.	Alcohol dependence	0	1	1	1
rs2104286	7E-6	5.15490195998574	19525955	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.	Multiple sclerosis	0	0	1	1
rs13015447	7E-6	5.15490195998574	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs2619566	7E-6	5.15490195998574	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	0	1	1	1
rs6494849	7E-6	5.15490195998574	19416921	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.	Bipolar disorder	1	1	1	1
rs153734	7E-6	5.15490195998574	19303062	Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations.	Folate pathway vitamin levels	1	1	1	1
rs758642	7E-6	5.15490195998574	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	1	1	1	1
rs2268983	7E-6	5.15490195998574	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	1	1	1	1
rs3027409	7E-6	5.15490195998574	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	NA	NA	NA	NA
rs10502868	7E-6	5.15490195998574	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	1	1	1	1
rs5982533	7E-6	5.15490195998574	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	NA	NA	NA	NA
rs267759	7E-6	5.15490195998574	19176441	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.	Response to treatment for acute lymphoblastic leukemia	1	1	1	1
rs2158836	7E-6	5.15490195998574	19122664	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.	Ulcerative colitis	0	0	0	0
rs29880	7E-6	5.15490195998574	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	1	1	1	1
rs12324805	7E-6	5.15490195998574	19079261	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.	Body mass index	1	1	1	1
rs4810685	7E-6	5.15490195998574	18937294	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.	Attention deficit hyperactivity disorder (time to onset)	0	1	1	1
rs2014572	7E-6	5.15490195998574	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Hyperactive-impulsive symptoms	1	1	1	1
rs13266634	7E-6	5.15490195998574	19056611	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data.	Type 2 diabetes	0	0	1	1
rs6917747	7E-6	5.15490195998574	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Brain lesion load	1	1	1	1
rs11666377	7E-6	5.15490195998574	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Brain lesion load	1	1	1	1
rs651477	7E-6	5.15490195998574	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs4704970	7E-6	5.15490195998574	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (age of onset)	1	1	1	1
rs9480865	7E-6	5.15490195998574	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Normalized brain volume	0	1	1	1
rs7595103	7E-6	5.15490195998574	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs789560	7E-6	5.15490195998574	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs16973500	7E-6	5.15490195998574	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	0	1	1	1
rs4889240	7E-6	5.15490195998574	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs11646411	7E-6	5.15490195998574	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	0	1	1	1
rs893971	7E-6	5.15490195998574	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	0	1	1	1
rs4321143	7E-6	5.15490195998574	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	0	1	1	1
rs2282301	7E-6	5.15490195998574	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	0	1	1	1
rs17664267	7E-6	5.15490195998574	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	0	1	1	1
rs2349775	7E-6	5.15490195998574	18762592	Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism.	Neuroticism	1	1	1	1
rs7226677	7E-6	5.15490195998574	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	0	1	1	1
rs1601875	7E-6	5.15490195998574	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	0	1	1	1
rs6761276	7E-6	5.15490195998574	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	1	1	1
rs7577642	7E-6	5.15490195998574	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	0	1	1	1
rs11265260	7E-6	5.15490195998574	18439552	Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein.	C-reactive protein	1	1	1	1
rs4345115	7E-6	5.15490195998574	18391951	Many sequence variants affecting diversity of adult human height.	Height	1	1	1	1
rs2808630	7E-6	5.15490195998574	18385676	Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1.	Lung cancer	0	1	1	1
rs8050136	7E-6	5.15490195998574	18372903	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.	Type 2 diabetes	0	0	1	1
rs12141391	7E-6	5.15490195998574	18204098	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.	Systemic lupus erythematosus	1	1	1	1
rs9322817	7E-6	5.15490195998574	17903292	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.	Thyroid stimulating hormone	0	1	1	1
rs499818	7E-6	5.15490195998574	17903304	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.	Major CVD	0	1	1	1
rs2509458	7E-6	5.15490195998574	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Blood pressure	1	1	1	1
rs7176093	7E-6	5.15490195998574	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Aging traits	1	1	1	1
rs7731657	7E-6	5.15490195998574	17903298	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	Fasting plasma glucose	0	1	1	1
rs1395479	7E-6	5.15490195998574	17903306	Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.	Heart rate variability traits	0	1	1	1
rs10507130	7E-6	5.15490195998574	17903303	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	Coronary artery calcification	0	1	1	1
rs1320267	7E-6	5.15490195998574	17903303	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	Subclinical atherosclerosis traits (other)	1	1	1	1
rs10493389	7E-6	5.15490195998574	17903301	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	Echocardiographic traits	0	1	1	1
rs4920799	7E-6	5.15490195998574	17903301	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	Echocardiographic traits	0	1	1	1
rs808225	7E-6	5.15490195998574	17903307	Framingham Heart Study genome-wide association: results for pulmonary function measures.	Pulmonary function	1	1	1	1
rs4129267	7E-6	5.15490195998574	17903307	Framingham Heart Study genome-wide association: results for pulmonary function measures.	Pulmonary function	0	1	1	1
rs10488360	7E-6	5.15490195998574	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Factor VII	1	1	1	1
rs2953145	7E-6	5.15490195998574	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Bipolar disorder	1	1	1	1
rs3761218	7E-6	5.15490195998574	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Bipolar disorder	0	0	1	1
rs10134944	7E-6	5.15490195998574	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Bipolar disorder	0	0	1	1
rs1495377	7E-6	5.15490195998574	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 2 diabetes	0	0	1	1
rs12304921	7E-6	5.15490195998574	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 2 diabetes	1	1	1	1
rs2797501	8E-6	5.09691001300806	23727862	Genome-wide association study identifies two susceptibility loci for osteosarcoma.	Osteosarcoma	1	1	1	1
rs2236835	8E-6	5.09691001300806	23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Body mass index	1	1	1	1
rs3733860	8E-6	5.09691001300806	23650146	A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Venous thromboembolism	1	1	1	1
rs3132946	8E-6	5.09691001300806	23583980	Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.	Interstitial lung disease 	0	1	1	1
rs6999631	8E-6	5.09691001300806	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	1	1	1	1
rs148915469	8E-6	5.09691001300806	23568457	Genetic variants associated with disordered eating.	Eating disorders	0	1	1	1
rs1506203	8E-6	5.09691001300806	23568457	Genetic variants associated with disordered eating.	Eating disorders (purging via substances) 	1	1	1	1
rs11603160	8E-6	5.09691001300806	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (asthmatics)	1	1	1	1
rs10771399	8E-6	5.09691001300806	23544013	Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.	Breast Cancer in BRCA1 mutation carriers	0	1	1	1
rs1449572	8E-6	5.09691001300806	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs7086888	8E-6	5.09691001300806	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs6601327	8E-6	5.09691001300806	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (hyperdiploidy)	0	0	0	0
rs649057	8E-6	5.09691001300806	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Smooth-surface caries 	0	1	1	1
rs1934620	8E-6	5.09691001300806	23470693	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	Smooth-surface caries 	1	1	1	1
rs1978746	8E-6	5.09691001300806	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	1	1	1	1
rs2273601	8E-6	5.09691001300806	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	0	1	1	1
rs9947295	8E-6	5.09691001300806	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	1	1	1	1
rs3817963	8E-6	5.09691001300806	23472185	Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.	Multiple sclerosis (OCB status)	0	0	0	0
rs360932	8E-6	5.09691001300806	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs3791556	8E-6	5.09691001300806	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs7597593	8E-6	5.09691001300806	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	1	1	1
rs6435387	8E-6	5.09691001300806	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs7849973	8E-6	5.09691001300806	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs10250997	8E-6	5.09691001300806	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs17267338	8E-6	5.09691001300806	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	0	1	1	1
rs17749211	8E-6	5.09691001300806	23412934	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs12155400	8E-6	5.09691001300806	23393555	Genome-wide association study of retinopathy in individuals without diabetes.	Retinopathy in non-diabetics	1	1	1	1
rs1329201	8E-6	5.09691001300806	23393555	Genome-wide association study of retinopathy in individuals without diabetes.	Retinopathy in non-diabetics	1	1	1	1
rs1457614	8E-6	5.09691001300806	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs974379	8E-6	5.09691001300806	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs12552369	8E-6	5.09691001300806	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	0	1	1	1
rs11055387	8E-6	5.09691001300806	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs1794265	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	NA	NA	NA	NA
rs17025548	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7902627	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11651000	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4376071	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs12431702	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs137699	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2862035	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1334809	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs3094093	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7953959	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7160685	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1853639	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs722599	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs10002492	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2540552	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs17124610	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1604897	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs6859704	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs17038828	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs255982	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7749924	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs12580533	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2028414	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6132333	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11169838	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs304172	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs3767633	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4684059	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9947954	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6494964	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11890081	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4972806	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs11910494	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs11958404	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1039443	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs918304	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs17348299	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2538958	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs604708	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs13021885	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7951911	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs9329350	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11899928	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs16839553	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs12528714	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10504390	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11675841	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2933343	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs435066	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10049992	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7301016	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs2072209	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6547115	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs16863118	8E-6	5.09691001300806	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs16932667	8E-6	5.09691001300806	23358156	Childhood intelligence is heritable, highly polygenic and associated with FNBP1L.	Intelligence (childhood)	1	1	1	1
rs12676170	8E-6	5.09691001300806	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs1278329	8E-6	5.09691001300806	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA/ MHPG Ratio)	1	1	1	1
rs2865126	8E-6	5.09691001300806	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA/ MHPG Ratio)	1	1	1	1
rs17834666	8E-6	5.09691001300806	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA)	0	1	0	0
rs6802119	8E-6	5.09691001300806	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA-5-HIAA Factor score)	NA	NA	NA	NA
rs284737	8E-6	5.09691001300806	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/5-HIAA ratio)	1	1	1	1
rs10798959	8E-6	5.09691001300806	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	0	1	1	1
rs2569872	8E-6	5.09691001300806	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs58938945	8E-6	5.09691001300806	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs13126513	8E-6	5.09691001300806	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs3785982	8E-6	5.09691001300806	23319801	Identification of inherited genetic variations influencing prognosis in early-onset breast cancer.	Breast cancer (prognosis)	1	1	1	1
rs2774307	8E-6	5.09691001300806	23319801	Identification of inherited genetic variations influencing prognosis in early-onset breast cancer.	Breast cancer (prognosis)	1	1	1	1
rs4293143	8E-6	5.09691001300806	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	1	1	1
rs6819266	8E-6	5.09691001300806	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	1	1	1	1
rs4714888	8E-6	5.09691001300806	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	1	1	1	1
rs17079247	8E-6	5.09691001300806	23326512	Genome-wide association study of irritable vs. elated mania suggests genetic differences between clinical subtypes of bipolar disorder.	Bipolar disorder (mania)	1	1	1	1
rs2128382	8E-6	5.09691001300806	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	1	1	1	1
rs4466078	8E-6	5.09691001300806	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs4922199	8E-6	5.09691001300806	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	0	0	1	1
rs10905651	8E-6	5.09691001300806	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs11172113	8E-6	5.09691001300806	23284291	Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.	Pulmonary function (interaction)	0	1	1	1
rs11886999	8E-6	5.09691001300806	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	1	1	1	1
rs9321637	8E-6	5.09691001300806	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	0	1	1	1
rs4806846	8E-6	5.09691001300806	23229837	TMPRSS9 and GRIN2B are associated with neuroticism: a genome-wide association study in a European sample.	Neuroticism	1	1	1	1
rs17290922	8E-6	5.09691001300806	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	1	1	1	1
rs6667220	8E-6	5.09691001300806	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	1	1	1	1
rs4468361	8E-6	5.09691001300806	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	1	1	1	1
rs7031748	8E-6	5.09691001300806	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	NA	NA	NA	NA
rs7578361	8E-6	5.09691001300806	23007406	Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	0	0	0	0
rs41322152	8E-6	5.09691001300806	23007406	Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	NA	NA	NA	NA
rs469568	8E-6	5.09691001300806	22990015	A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke.	Stroke (pediatric)	1	1	1	1
rs2657195	8E-6	5.09691001300806	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs11754641	8E-6	5.09691001300806	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs2834902	8E-6	5.09691001300806	22969067	Genetic variants near PDGFRA are associated with corneal curvature in Australians.	Corneal curvature	1	1	1	1
rs1912785	8E-6	5.09691001300806	22961001	Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.	Barrett's esophagus	1	1	1	1
rs1421746	8E-6	5.09691001300806	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis (age of onset)	0	1	1	1
rs1491818	8E-6	5.09691001300806	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis (age of onset)	1	1	1	1
rs2036225	8E-6	5.09691001300806	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis (age of onset)	1	1	1	1
rs41458646	8E-6	5.09691001300806	22881374	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	Alzheimer's disease (late onset)	1	1	1	1
rs17767225	8E-6	5.09691001300806	22881374	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	Alzheimer's disease (late onset)	0	0	0	0
rs2048485	8E-6	5.09691001300806	22885689	Genome-wide association study of multiplex schizophrenia pedigrees.	Schizophrenia	1	1	1	1
rs7897194	8E-6	5.09691001300806	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	1	1	1	1
rs6510489	8E-6	5.09691001300806	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	1	1	1	1
rs1898111	8E-6	5.09691001300806	22911880	Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits.	Eating disorders	1	1	1	1
rs17140547	8E-6	5.09691001300806	22903471	Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.	Lentiform nucleus volume 	1	1	1	1
rs9393366	8E-6	5.09691001300806	22889924	Genome-wide association study of Tourette's syndrome.	Tourette syndrome	1	1	1	1
rs9611198	8E-6	5.09691001300806	22883433	Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia.	Schizophrenia	0	1	1	1
rs2322734	8E-6	5.09691001300806	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs8036030	8E-6	5.09691001300806	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	0	1	1	1
rs1791933	8E-6	5.09691001300806	22754043	A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.	Insomnia (caffeine-induced)	1	1	1	1
rs10488023	8E-6	5.09691001300806	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs253959	8E-6	5.09691001300806	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs17029069	8E-6	5.09691001300806	22683750	A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern.	Cardiac repolarization	0	1	1	1
rs12059860	8E-6	5.09691001300806	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Testosterone levels	1	1	1	1
rs732949	8E-6	5.09691001300806	22658931	A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed.	Immune response to anthrax vaccine 	1	1	1	1
rs10758161	8E-6	5.09691001300806	22658931	A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed.	Immune response to anthrax vaccine 	1	1	1	1
rs13037749	8E-6	5.09691001300806	22745009	Multiple loci influencing hippocampal degeneration identified by genome scan.	Hippocampal atrophy	1	1	1	1
rs13153333	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs4886088	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs11757661	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs4304868	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs6946494	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs7324557	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs4657015	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs7638389	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	0	1	0	0
rs10516635	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	0	1	1	1
rs1498095	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs7547921	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs13177918	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs1791581	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs2267193	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs962528	8E-6	5.09691001300806	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	0	1	0	0
rs784420	8E-6	5.09691001300806	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs13068298	8E-6	5.09691001300806	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (feminism/equality)	0	0	0	0
rs10511400	8E-6	5.09691001300806	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (feminism/equality)	1	1	1	1
rs9364813	8E-6	5.09691001300806	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	1	1	1	1
rs12619788	8E-6	5.09691001300806	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	0	1	1	1
rs11178918	8E-6	5.09691001300806	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (time)	0	0	0	0
rs960902	8E-6	5.09691001300806	22569225	Investigation of single nucleotide polymorphisms and biological pathways associated with response to TNFα inhibitors in patients with rheumatoid arthritis.	Response to TNF-alpha inhibitors in rheumatoid arthritis	0	1	1	1
rs4256430	8E-6	5.09691001300806	22554406	Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6.	Electroencephalographic traits in alcoholism	NA	NA	NA	NA
rs7667	8E-6	5.09691001300806	22482804	Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.	Crohn's disease and psoriasis	0	1	1	1
rs2721937	8E-6	5.09691001300806	22472876	A mega-analysis of genome-wide association studies for major depressive disorder.	Major depressive disorder	0	1	1	1
rs2657888	8E-6	5.09691001300806	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	1	1	1	1
rs12615721	8E-6	5.09691001300806	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	0	1	1	1
rs7313402	8E-6	5.09691001300806	22365631	Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.	Temperament (bipolar disorder)	1	1	1	1
rs8105815	8E-6	5.09691001300806	22210626	Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.	Prion diseases	1	1	1	1
rs13230047	8E-6	5.09691001300806	22216198	A genome-wide association study of the Protein C anticoagulant pathway.	Anticoagulant levels	1	1	1	1
rs1006973	8E-6	5.09691001300806	22216198	A genome-wide association study of the Protein C anticoagulant pathway.	Anticoagulant levels	1	1	1	1
rs1401543	8E-6	5.09691001300806	22216198	A genome-wide association study of the Protein C anticoagulant pathway.	Anticoagulant levels	1	1	1	1
rs11062040	8E-6	5.09691001300806	22142827	A genome-wide association study of overall survival in pancreatic cancer patients treated with gemcitabine in CALGB 80303.	Response to gemcitabine in pancreatic cancer 	1	1	1	1
rs10504906	8E-6	5.09691001300806	21897333	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	Fat distribution (HIV)	0	0	0	0
rs11725957	8E-6	5.09691001300806	22095909	Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.	Response to hepatitis C treatment	1	1	1	1
rs282708	8E-6	5.09691001300806	22076464	Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs17750015	8E-6	5.09691001300806	22064162	Genome-wide association study of comorbid depressive syndrome and alcohol dependence.	Depression and alcohol dependence	1	1	1	1
rs10090288	8E-6	5.09691001300806	22064162	Genome-wide association study of comorbid depressive syndrome and alcohol dependence.	Depression and alcohol dependence	1	1	1	1
rs12785341	8E-6	5.09691001300806	22044751	Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study.	Renal sinus fat 	0	1	1	1
rs6686423	8E-6	5.09691001300806	22044751	Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study.	Renal sinus fat 	1	1	1	1
rs9825310	8E-6	5.09691001300806	22004471	Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.	Alcohol dependence	1	1	1	1
rs12933233	8E-6	5.09691001300806	22005931	Genome-wide association analysis of age-at-onset in Alzheimer's disease.	Alzheimer's disease (age of onset)	1	1	1	1
rs1037757	8E-6	5.09691001300806	22005931	Genome-wide association analysis of age-at-onset in Alzheimer's disease.	Alzheimer's disease (age of onset)	1	1	1	1
rs17077154	8E-6	5.09691001300806	21993531	Genome-wide association study does not reveal major genetic determinants for anti-cytomegalovirus antibody response.	Cytomegalovirus antibody response	1	1	1	1
rs10893366	8E-6	5.09691001300806	21956439	Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q.	Alcohol dependence	0	0	1	1
rs9636231	8E-6	5.09691001300806	21956439	Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q.	Alcohol dependence	1	1	1	1
rs4762767	8E-6	5.09691001300806	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs11031093	8E-6	5.09691001300806	21940522	Genome-wide association scan for childhood caries implicates novel genes.	Dental caries	0	1	1	1
rs2302189	8E-6	5.09691001300806	21940522	Genome-wide association scan for childhood caries implicates novel genes.	Dental caries	0	1	1	1
rs2932538	8E-6	5.09691001300806	21909110	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.	Blood pressure	0	1	1	1
rs3119939	8E-6	5.09691001300806	21907864	Identification of IL6R and chromosome 11q13.5 as risk loci for asthma.	Asthma	1	1	1	1
rs12344583	8E-6	5.09691001300806	21810271	Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.	vWF and FVIII levels	1	1	1	1
rs10202497	8E-6	5.09691001300806	21782286	A genome-wide association study of aging.	Aging (time to event)	1	1	1	1
rs797820	8E-6	5.09691001300806	21784300	Genome-wide association study of the child behavior checklist dysregulation profile.	Attention deficit hyperactivity disorder	0	1	1	1
rs758944	8E-6	5.09691001300806	21654844	Genome-wide association study of severity in multiple sclerosis.	Multiple sclerosis	0	0	0	0
rs7779014	8E-6	5.09691001300806	21654844	Genome-wide association study of severity in multiple sclerosis.	Multiple sclerosis	0	0	0	0
rs11962089	8E-6	5.09691001300806	21654844	Genome-wide association study of severity in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs12883884	8E-6	5.09691001300806	21602797	Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.	Cystic fibrosis severity	1	1	1	1
rs3930234	8E-6	5.09691001300806	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (alcohol use disorder factor score)	1	1	1	1
rs768048	8E-6	5.09691001300806	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (alcohol use disorder factor score)	1	1	1	1
rs2827312	8E-6	5.09691001300806	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (heaviness of drinking)	1	1	1	1
rs2306029	8E-6	5.09691001300806	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	0	1	1	1
rs1351696	8E-6	5.09691001300806	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	NA	NA	NA	NA
rs3811647	8E-6	5.09691001300806	21483845	Genome-wide association study identifies genetic loci associated with iron deficiency.	Iron status biomarkers	0	0	0	0
rs140174	8E-6	5.09691001300806	21448238	Meta-analysis of genome-wide association for migraine in six population-based European cohorts.	Migraine	1	1	1	1
rs1463525	8E-6	5.09691001300806	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	1	1	1	1
rs7574865	8E-6	5.09691001300806	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	0	0	0	0
rs6049839	8E-6	5.09691001300806	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	1	1	1	1
rs2647012	8E-6	5.09691001300806	21408207	Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.	Systemic lupus erythematosus	0	0	0	0
rs2286492	8E-6	5.09691001300806	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs2206734	8E-6	5.09691001300806	21139019	A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum.	Ileal carcinoids	0	1	1	1
rs1375785	8E-6	5.09691001300806	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs4815868	8E-6	5.09691001300806	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs11077773	8E-6	5.09691001300806	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs17774966	8E-6	5.09691001300806	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Entorhinal cortical thickness	1	1	1	1
rs9846480	8E-6	5.09691001300806	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	MRI atrophy measures	0	1	1	1
rs4479806	8E-6	5.09691001300806	21079607	A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.	Anorexia nervosa	1	1	1	1
rs957788	8E-6	5.09691001300806	21079607	A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.	Anorexia nervosa	1	1	1	1
rs12811699	8E-6	5.09691001300806	21668797	A genome-wide association study of DSM-IV cannabis dependence.	Cannabis dependence	1	1	1	1
rs9507041	8E-6	5.09691001300806	21668797	A genome-wide association study of DSM-IV cannabis dependence.	Cannabis dependence	1	1	1	1
rs28372448	8E-6	5.09691001300806	21668797	A genome-wide association study of DSM-IV cannabis dependence.	Cannabis dependence	NA	NA	NA	NA
rs11210359	8E-6	5.09691001300806	21057379	Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes.	Bipolar disorder and schizophrenia	1	1	1	1
rs6459804	8E-6	5.09691001300806	21057379	Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes.	Bipolar disorder and schizophrenia	1	1	1	1
rs929351	8E-6	5.09691001300806	20848476	Genetic predictors of medically refractory ulcerative colitis.	Ulcerative colitis	0	1	1	1
rs278567	8E-6	5.09691001300806	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs2235121	8E-6	5.09691001300806	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1092015	8E-6	5.09691001300806	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1605834	8E-6	5.09691001300806	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs16822582	8E-6	5.09691001300806	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs7941534	8E-6	5.09691001300806	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs830407	8E-6	5.09691001300806	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs17699030	8E-6	5.09691001300806	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs12280753	8E-6	5.09691001300806	20838585	Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.	Cardiovascular disease risk factors	0	1	1	1
rs9831754	8E-6	5.09691001300806	20705733	Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.	Calcium levels	0	1	1	1
rs11083271	8E-6	5.09691001300806	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (lobular)	1	1	1	1
rs12753569	8E-6	5.09691001300806	20691247	A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality.	Personality dimensions	0	1	1	1
rs7279441	8E-6	5.09691001300806	20707712	A genome-wide association study of self-rated health.	Self-rated health	1	1	1	1
rs10485813	8E-6	5.09691001300806	20732625	Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	0	1	1	1
rs10011926	8E-6	5.09691001300806	20732626	Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	1	1	1	1
rs11203032	8E-6	5.09691001300806	20445134	Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.	Heart failure	1	1	1	1
rs1010254	8E-6	5.09691001300806	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (cup)	1	1	1	1
rs8000245	8E-6	5.09691001300806	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (rim)	0	1	1	1
rs6830062	8E-6	5.09691001300806	20397748	Genome-wide association study of height and body mass index in Australian twin families.	Height	0	0	1	1
rs1395241	8E-6	5.09691001300806	20351715	Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.	Bipolar disorder and major depressive disorder (combined)	1	1	1	1
rs1262778	8E-6	5.09691001300806	20351715	Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.	Bipolar disorder and major depressive disorder (combined)	0	1	1	1
rs6588480	8E-6	5.09691001300806	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs729397	8E-6	5.09691001300806	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs35964523	8E-6	5.09691001300806	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	0	0	0	0
rs7900909	8E-6	5.09691001300806	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs541041	8E-6	5.09691001300806	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	0	1	1	1
rs10266483	8E-6	5.09691001300806	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs11641231	8E-6	5.09691001300806	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	0	1	1	1
rs9305406	8E-6	5.09691001300806	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs16917919	8E-6	5.09691001300806	20197096	Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.	Brain structure (hippocampal volume)	1	1	1	1
rs7155434	8E-6	5.09691001300806	20197096	Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.	Brain structure (temporal lobe volume)	0	1	1	1
rs12424086	8E-6	5.09691001300806	20195514	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Primary tooth development (time to first tooth eruption)	0	0	0	0
rs10761482	8E-6	5.09691001300806	20185149	Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort.	Schizophrenia	1	1	1	1
rs12117544	8E-6	5.09691001300806	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs17275498	8E-6	5.09691001300806	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs7659062	8E-6	5.09691001300806	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs7662358	8E-6	5.09691001300806	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	0	0	0	0
rs7782376	8E-6	5.09691001300806	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	NA	NA	NA	NA
rs2978263	8E-6	5.09691001300806	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs11232369	8E-6	5.09691001300806	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	0	1	1	1
rs12797755	8E-6	5.09691001300806	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs2058350	8E-6	5.09691001300806	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs4815617	8E-6	5.09691001300806	20159242	Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions.	Asthma	1	1	1	1
rs958994	8E-6	5.09691001300806	20009918	A genome-wide association study of carotid atherosclerosis in HIV-infected men.	Carotid atherosclerosis in HIV infection	1	1	1	1
rs588517	8E-6	5.09691001300806	20009918	A genome-wide association study of carotid atherosclerosis in HIV-infected men.	Carotid atherosclerosis in HIV infection	0	1	1	1
rs10928302	8E-6	5.09691001300806	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs1463132	8E-6	5.09691001300806	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs1454292	8E-6	5.09691001300806	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	1	1	1	1
rs1816002	8E-6	5.09691001300806	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Weight	0	1	1	1
rs4947019	8E-6	5.09691001300806	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Hematological parameters	0	1	1	1
rs10918270	8E-6	5.09691001300806	19772629	Genomewide association study for onset age in Parkinson disease.	Parkinson's disease (age of onset)	1	1	1	1
rs4430796	8E-6	5.09691001300806	19767754	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.	Prostate cancer	0	0	1	1
rs6486986	8E-6	5.09691001300806	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs16851254	8E-6	5.09691001300806	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs4083578	8E-6	5.09691001300806	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	0	1	1	1
rs1820460	8E-6	5.09691001300806	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs4284125	8E-6	5.09691001300806	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	NA	NA	NA	NA
rs7984606	8E-6	5.09691001300806	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs11032423	8E-6	5.09691001300806	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs8085804	8E-6	5.09691001300806	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs7892812	8E-6	5.09691001300806	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	NA	NA	NA	NA
rs12612420	8E-6	5.09691001300806	19727025	Genome-wide association study of exercise behavior in Dutch and American adults.	Exercise (leisure time)	0	1	1	1
rs17067123	8E-6	5.09691001300806	19684573	Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance.	Response to hepatitis C treatment	1	1	1	1
rs682748	8E-6	5.09691001300806	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs7727656	8E-6	5.09691001300806	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs9918508	8E-6	5.09691001300806	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs1373549	8E-6	5.09691001300806	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs6902771	8E-6	5.09691001300806	19581569	Genome-wide association study of alcohol dependence.	Alcohol dependence	0	1	1	1
rs7603514	8E-6	5.09691001300806	19553259	Common body mass index-associated variants confer risk of extreme obesity.	Obesity (extreme)	1	1	1	1
rs907092	8E-6	5.09691001300806	19458352	Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.	Primary biliary cirrhosis	0	0	1	1
rs16856202	8E-6	5.09691001300806	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs873917	8E-6	5.09691001300806	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs7702057	8E-6	5.09691001300806	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	0	1	1	1
rs8066857	8E-6	5.09691001300806	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs3099950	8E-6	5.09691001300806	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs4773330	8E-6	5.09691001300806	19414484	Genome-wide association meta-analysis for total serum bilirubin levels.	Bilirubin levels	1	1	1	1
rs11646213	8E-6	5.09691001300806	19304780	Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations.	Hypertension	1	1	1	1
rs17050782	8E-6	5.09691001300806	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	1	1	1	1
rs912969	8E-6	5.09691001300806	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	1	1	1	1
rs1847461	8E-6	5.09691001300806	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	1	1	1	1
rs886716	8E-6	5.09691001300806	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	0	1	1	1
rs1863080	8E-6	5.09691001300806	19260139	Genome-wide association study of anthropometric traits in Korcula Island, Croatia.	Anthropometric traits	1	1	1	1
rs2839619	8E-6	5.09691001300806	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	0	1	1	1
rs6044777	8E-6	5.09691001300806	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	1	1	1	1
rs10508343	8E-6	5.09691001300806	19176441	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.	Response to treatment for acute lymphoblastic leukemia	NA	NA	NA	NA
rs7115578	8E-6	5.09691001300806	19176441	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.	Response to treatment for acute lymphoblastic leukemia	0	1	1	1
rs13188386	8E-6	5.09691001300806	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	1	1	1
rs2052550	8E-6	5.09691001300806	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	1	1	1	1
rs2660917	8E-6	5.09691001300806	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	1	1	1	1
rs7481311	8E-6	5.09691001300806	19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Body mass index	0	0	0	0
rs10889353	8E-6	5.09691001300806	19060911	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.	LDL cholesterol	0	0	0	0
rs1350666	8E-6	5.09691001300806	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	0	1	1	1
rs260461	8E-6	5.09691001300806	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	1	1	1	1
rs10767942	8E-6	5.09691001300806	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	1	1	1	1
rs6791644	8E-6	5.09691001300806	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	0	1	1	1
rs10039254	8E-6	5.09691001300806	18937294	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.	Attention deficit hyperactivity disorder (time to onset)	1	1	1	1
rs1335515	8E-6	5.09691001300806	18937294	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.	Attention deficit hyperactivity disorder (time to onset)	0	1	1	1
rs1018040	8E-6	5.09691001300806	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Hyperactive-impulsive symptoms	0	1	0	0
rs6808138	8E-6	5.09691001300806	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Hyperactive-impulsive symptoms	0	0	0	0
rs4147141	8E-6	5.09691001300806	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	0	0	0	0
rs478597	8E-6	5.09691001300806	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	NA	NA	NA	NA
rs1471225	8E-6	5.09691001300806	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	1	1	1	1
rs644148	8E-6	5.09691001300806	18957941	Genome-wide association scan for five major dimensions of personality.	Personality dimensions	0	0	0	0
rs7672826	8E-6	5.09691001300806	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs1841770	8E-6	5.09691001300806	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs1437898	8E-6	5.09691001300806	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (age of onset)	1	1	1	1
rs1927457	8E-6	5.09691001300806	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Normalized brain volume	1	1	1	1
rs716595	8E-6	5.09691001300806	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Normalized brain volume	1	1	1	1
rs6427356	8E-6	5.09691001300806	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs1521882	8E-6	5.09691001300806	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs1644305	8E-6	5.09691001300806	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs2242073	8E-6	5.09691001300806	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs2241685	8E-6	5.09691001300806	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs469727	8E-6	5.09691001300806	18839057	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Attention deficit hyperactivity disorder	1	1	1	1
rs2825388	8E-6	5.09691001300806	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Attention deficit hyperactivity disorder symptoms (interaction)	1	1	1	1
rs10049246	8E-6	5.09691001300806	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Attention deficit hyperactivity disorder symptoms (interaction)	0	1	1	1
rs2360997	8E-6	5.09691001300806	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Attention deficit hyperactivity disorder symptoms (interaction)	1	1	1	1
rs8073783	8E-6	5.09691001300806	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	1	1	1	1
rs604381	8E-6	5.09691001300806	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	NA	NA	NA	NA
rs3776331	8E-6	5.09691001300806	18759275	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish.	Uric acid levels	1	1	1	1
rs703965	8E-6	5.09691001300806	18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Bipolar disorder	0	1	1	1
rs2313132	8E-6	5.09691001300806	19165918	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.	Systemic lupus erythematosus	1	1	1	1
rs12949531	8E-6	5.09691001300806	19165918	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.	Systemic lupus erythematosus	1	1	1	1
rs3885683	8E-6	5.09691001300806	18464913	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Protein quantitative trait loci	1	1	1	1
rs31198	8E-6	5.09691001300806	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs9395066	8E-6	5.09691001300806	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs1239947	8E-6	5.09691001300806	18391951	Many sequence variants affecting diversity of adult human height.	Height	0	0	1	1
rs17104630	8E-6	5.09691001300806	18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Height	1	1	1	1
rs7626795	8E-6	5.09691001300806	18385676	Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1.	Lung cancer	1	1	1	1
rs1333026	8E-6	5.09691001300806	17903300	Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.	Body mass index	1	1	1	1
rs10499559	8E-6	5.09691001300806	17903292	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.	Thyroid stimulating hormone	1	1	1	1
rs9305354	8E-6	5.09691001300806	17903292	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.	Urinary albumin excretion	1	1	1	1
rs4776472	8E-6	5.09691001300806	17903304	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.	Atrial fibrillation	0	1	1	1
rs1322512	8E-6	5.09691001300806	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Tonometry	1	1	1	1
rs10488172	8E-6	5.09691001300806	17903302	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Tonometry	1	1	1	1
rs3772255	8E-6	5.09691001300806	17903295	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Aging traits	1	1	1	1
rs10486607	8E-6	5.09691001300806	17903298	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	Diabetes related insulin traits	1	1	1	1
rs10507380	8E-6	5.09691001300806	17903306	Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.	Electrocardiographic traits	1	1	1	1
rs9315385	8E-6	5.09691001300806	17903306	Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.	Heart rate variability traits	0	1	1	1
rs9300212	8E-6	5.09691001300806	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Cognitive test performance	0	1	1	1
rs1831521	8E-6	5.09691001300806	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Cognitive test performance	1	1	1	1
rs2906966	8E-6	5.09691001300806	17903307	Framingham Heart Study genome-wide association: results for pulmonary function measures.	Pulmonary function	1	1	1	1
rs966321	8E-6	5.09691001300806	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Factor VII	1	1	1	1
rs727979	8E-6	5.09691001300806	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Hemostatic factors and hematological phenotypes	0	0	0	0
rs6604026	8E-6	5.09691001300806	17660530	Risk alleles for multiple sclerosis identified by a genomewide study.	Multiple sclerosis	0	0	1	1
rs10984447	8E-6	5.09691001300806	17660530	Risk alleles for multiple sclerosis identified by a genomewide study.	Multiple sclerosis	0	1	1	1
rs11622475	8E-6	5.09691001300806	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Bipolar disorder	0	0	1	1
rs1445898	8E-6	5.09691001300806	17554260	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.	Type 1 diabetes	0	1	1	1
rs6897932	8E-6	5.09691001300806	17554260	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.	Type 1 diabetes	0	0	0	0
rs7702187	8E-6	5.09691001300806	16252231	High-resolution whole-genome association study of Parkinson disease.	Parkinson's disease	1	1	1	1
rs573666	9E-6	5.04575749056067	23727862	Genome-wide association study identifies two susceptibility loci for osteosarcoma.	Osteosarcoma	0	1	1	1
rs2210430	9E-6	5.04575749056067	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep quality	1	1	1	1
rs1949200	9E-6	5.04575749056067	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep quality	0	1	1	1
rs7195303	9E-6	5.04575749056067	23665963	Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease.	Crohn's disease (time to surgery)	1	1	1	1
rs553169	9E-6	5.04575749056067	23577725	Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.	Age-related macular degeneration (smoking status interaction)	1	1	1	1
rs55946907	9E-6	5.04575749056067	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	1	1	1	1
rs9531686	9E-6	5.04575749056067	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	1	1	1	1
rs28441017	9E-6	5.04575749056067	23568457	Genetic variants associated with disordered eating.	Anorexia nervosa	1	1	1	1
rs117124364	9E-6	5.04575749056067	23568457	Genetic variants associated with disordered eating.	Bulimia nervosa	NA	NA	NA	NA
rs12408810	9E-6	5.04575749056067	23563609	Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.	Obesity (early onset extreme)	1	1	1	1
rs4141232	9E-6	5.04575749056067	23593202	Bivariate genome-wide association analyses identified genes with pleiotropic effects for femoral neck bone geometry and age at menarche.	Femoral neck bone geometry and menarche (age at onset)	0	0	0	0
rs17166082	9E-6	5.04575749056067	23593239	The molecular genetic architecture of self-employment.	Self-employment	1	1	1	1
rs17356907	9E-6	5.04575749056067	23535733	Genome-wide association studies identify four ER negative-specific breast cancer risk loci.	Breast cancer	0	0	1	1
rs12468557	9E-6	5.04575749056067	23517042	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Body mass index (asthmatics)	1	1	1	1
rs12984174	9E-6	5.04575749056067	23541324	Genome-wide association study identifies TH1 pathway genes associated with lung function in asthmatic patients.	Pulmonary function in asthmatics	1	1	1	1
rs6988229	9E-6	5.04575749056067	23508266	A genome-wide association study of bronchodilator response in asthmatics.	Asthma (bronchodilator response)	1	1	1	1
rs7144018	9E-6	5.04575749056067	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs4521323	9E-6	5.04575749056067	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	1	1	1	1
rs139371	9E-6	5.04575749056067	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	0	1	0	0
rs7536700	9E-6	5.04575749056067	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (IgH translocation)	0	0	0	0
rs9864370	9E-6	5.04575749056067	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (hyperdiploidy)	0	1	1	1
rs11026318	9E-6	5.04575749056067	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (hyperdiploidy)	1	1	1	1
rs11157317	9E-6	5.04575749056067	23502783	The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.	Multiple myeloma (hyperdiploidy)	1	1	1	1
rs129963	9E-6	5.04575749056067	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	1	1	1	1
rs13437751	9E-6	5.04575749056067	23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	QT interval (interaction)	1	1	1	1
rs1533087	9E-6	5.04575749056067	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	1	1	1	1
rs13072940	9E-6	5.04575749056067	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	0	0	0	0
rs7742824	9E-6	5.04575749056067	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs4625554	9E-6	5.04575749056067	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	0	1	1	1
rs2377360	9E-6	5.04575749056067	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	1	1	1	1
rs2462686	9E-6	5.04575749056067	23377640	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Major depressive disorder	0	1	1	1
rs909674	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4760854	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs2692194	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs918304	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11899928	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10971170	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs3763048	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4852708	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10519937	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs1436958	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs592229	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2659005	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1368304	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs7249142	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs10877839	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs3851357	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1319535	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs6983039	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11825685	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2664299	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2965260	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11651000	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs7845056	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4789580	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11212260	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1953652	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2844479	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2677247	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs1475911	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs27323	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4954683	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs6059594	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs9832314	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs10065350	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs4862046	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs11779594	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs2745851	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs2937550	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11706018	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs4699982	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	1	1	1
rs8010715	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs11635553	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	0	0	0	0
rs13245023	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs1035275	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs672561	9E-6	5.04575749056067	23382691	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	IgG glycosylation	1	1	1	1
rs470089	9E-6	5.04575749056067	23386860	Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes.	Type 2 diabetes (dietary heme iron intake interaction)	1	1	1	1
rs6540731	9E-6	5.04575749056067	23358156	Childhood intelligence is heritable, highly polygenic and associated with FNBP1L.	Intelligence (childhood)	1	1	1	1
rs13387221	9E-6	5.04575749056067	23358156	Childhood intelligence is heritable, highly polygenic and associated with FNBP1L.	Intelligence (childhood)	1	1	1	1
rs4961511	9E-6	5.04575749056067	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs11098499	9E-6	5.04575749056067	23322567	Identification of a candidate gene for astigmatism.	Corneal astigmatism	1	1	1	1
rs4949316	9E-6	5.04575749056067	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA)	1	1	1	1
rs78867184	9E-6	5.04575749056067	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA)	1	1	1	1
rs35212277	9E-6	5.04575749056067	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA/ MHPG Ratio)	1	1	1	1
rs2006970	9E-6	5.04575749056067	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (5-HIAA/ MHPG Ratio)	1	1	1	1
rs141215807	9E-6	5.04575749056067	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA)	1	1	1	1
rs114646238	9E-6	5.04575749056067	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (HVA/MHPG ratio)	1	1	1	1
rs13303128	9E-6	5.04575749056067	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs144649413	9E-6	5.04575749056067	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	1	1	1	1
rs4559365	9E-6	5.04575749056067	23319000	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	Metabolite levels (MHPG)	NA	NA	NA	NA
rs2049622	9E-6	5.04575749056067	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	1	1	1	1
rs10830228	9E-6	5.04575749056067	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	0	0	0
rs584480	9E-6	5.04575749056067	23263486	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Urate levels	0	1	1	1
rs1912453	9E-6	5.04575749056067	23266556	Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.	Colorectal cancer	1	1	1	1
rs4865673	9E-6	5.04575749056067	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs7243066	9E-6	5.04575749056067	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs1163656	9E-6	5.04575749056067	23259602	Genome-wide association scan of dental caries in the permanent dentition.	Dental caries	1	1	1	1
rs17724172	9E-6	5.04575749056067	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	1	1	1	1
rs17666963	9E-6	5.04575749056067	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	1	1	1	1
rs959770	9E-6	5.04575749056067	23212062	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	Schizophrenia	1	1	1	1
rs9783347	9E-6	5.04575749056067	23180869	Genome-wide association study of survival in patients with pancreatic adenocarcinoma.	Pancreatic cancer	0	1	1	1
rs1124480	9E-6	5.04575749056067	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	NA	NA	NA	NA
rs1930961	9E-6	5.04575749056067	23092984	Genome-wide association of mood-incongruent psychotic bipolar disorder.	Bipolar disorder (mood-incongruent)	1	1	1	1
rs10758892	9E-6	5.04575749056067	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	1	1	1	1
rs4149311	9E-6	5.04575749056067	23049088	A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.	Myopia (pathological)	0	1	1	1
rs546784	9E-6	5.04575749056067	23007406	Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	0	0	0	0
rs13045180	9E-6	5.04575749056067	23028342	New susceptibility loci associated with kidney disease in type 1 diabetes.	Type 1 diabetes nephropathy	1	1	1	1
rs12805875	9E-6	5.04575749056067	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	1	1	1	1
rs980238	9E-6	5.04575749056067	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs7103004	9E-6	5.04575749056067	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	NA	NA	NA	NA
rs4554859	9E-6	5.04575749056067	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs7118412	9E-6	5.04575749056067	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs2017567	9E-6	5.04575749056067	22993228	Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.	Disc degeneration (lumbar)	0	0	0	0
rs1869463	9E-6	5.04575749056067	22969067	Genetic variants near PDGFRA are associated with corneal curvature in Australians.	Corneal curvature	1	1	1	1
rs17137734	9E-6	5.04575749056067	22969067	Genetic variants near PDGFRA are associated with corneal curvature in Australians.	Corneal curvature	1	1	1	1
rs1531228	9E-6	5.04575749056067	22961001	Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.	Barrett's esophagus	1	1	1	1
rs7665939	9E-6	5.04575749056067	22959728	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	Amyotrophic lateral sclerosis	1	1	1	1
rs12720541	9E-6	5.04575749056067	22949513	Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32	Epilepsy (generalized)	1	1	1	1
rs6085820	9E-6	5.04575749056067	22881374	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	Alzheimer's disease (late onset)	1	1	1	1
rs1170612	9E-6	5.04575749056067	22885689	Genome-wide association study of multiplex schizophrenia pedigrees.	Schizophrenia	0	0	0	0
rs312273	9E-6	5.04575749056067	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	1	1	1	1
rs6124684	9E-6	5.04575749056067	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	1	1	1	1
rs6027511	9E-6	5.04575749056067	22903471	Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.	Lentiform nucleus volume 	0	1	1	1
rs10918196	9E-6	5.04575749056067	22903471	Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.	Lentiform nucleus volume 	1	1	1	1
rs621942	9E-6	5.04575749056067	22889924	Genome-wide association study of Tourette's syndrome.	Tourette syndrome	0	1	1	1
rs7820074	9E-6	5.04575749056067	22863734	Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.	Orofacial clefts	1	1	1	1
rs7629245	9E-6	5.04575749056067	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	0	1	1	1
rs892961	9E-6	5.04575749056067	22837378	Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.	Airflow obstruction 	1	1	1	1
rs11010290	9E-6	5.04575749056067	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	1	1	1	1
rs11079740	9E-6	5.04575749056067	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	1	1	1	1
rs1572438	9E-6	5.04575749056067	22773346	Linkage and association of successful aging to the 6q25 region in large Amish kindreds.	Aging	1	1	1	1
rs643473	9E-6	5.04575749056067	22773346	Linkage and association of successful aging to the 6q25 region in large Amish kindreds.	Aging	1	1	1	1
rs16905439	9E-6	5.04575749056067	22754043	A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.	Insomnia (caffeine-induced)	1	1	1	1
rs6549915	9E-6	5.04575749056067	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	1	1	1	1
rs58263042	9E-6	5.04575749056067	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	NA	NA	NA	NA
rs2058710	9E-6	5.04575749056067	22688191	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1712517	9E-6	5.04575749056067	22683712	Genome-wide association analysis identifies susceptibility loci for migraine without aura.	Migraine	0	1	1	1
rs12596210	9E-6	5.04575749056067	22675492	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Sex hormone-binding globulin levels	1	1	1	1
rs7526035	9E-6	5.04575749056067	22648509	PKNOX2 is associated with formal thought disorder in schizophrenia: a meta-analysis of two genome-wide association studies.	Formal thought disorder in schizophrenia	1	1	1	1
rs3027247	9E-6	5.04575749056067	22658654	Genomic determinants of motor and cognitive outcomes in Parkinson's disease.	Parkinson's disease (motor and cognition)	0	1	1	1
rs2647264	9E-6	5.04575749056067	22658931	A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed.	Immune response to anthrax vaccine 	0	1	1	1
rs1357692	9E-6	5.04575749056067	22832961	Genome-wide association study of Alzheimer's disease.	Alzheimer's disease	1	1	1	1
rs10057405	9E-6	5.04575749056067	22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Temperament	0	1	1	1
rs6686886	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs870288	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	0	1	1	1
rs11858577	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs12185578	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Subcutaneous adipose tissue	1	1	1	1
rs1048497	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	0	0	0	0
rs2777777	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	0	1	0	0
rs6789987	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	0	1	0	0
rs901254	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue adjusted for BMI	1	1	1	1
rs7042950	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	0	1	1	1
rs6464816	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs9861887	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral adipose tissue/subcutaneous adipose tissue ratio	1	1	1	1
rs6504663	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs7336109	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs2001970	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	0	1	1	1
rs17022027	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs9375969	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs12285276	9E-6	5.04575749056067	22589738	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Visceral fat	1	1	1	1
rs7209847	9E-6	5.04575749056067	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences	1	1	1	1
rs4838320	9E-6	5.04575749056067	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (immigration/crime)	1	1	1	1
rs9728717	9E-6	5.04575749056067	22566634	The genetic architecture of economic and political preferences.	Economic and political preferences (time)	0	1	1	1
rs17679567	9E-6	5.04575749056067	22569225	Investigation of single nucleotide polymorphisms and biological pathways associated with response to TNFα inhibitors in patients with rheumatoid arthritis.	Response to TNF-alpha inhibitors in rheumatoid arthritis	1	1	1	1
rs229526	9E-6	5.04575749056067	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	0	1	1	1
rs3748682	9E-6	5.04575749056067	22493691	Novel associations for hypothyroidism include known autoimmune risk loci.	Hypothyroidism	1	1	1	1
rs13434995	9E-6	5.04575749056067	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	0	1	1	1
rs4777845	9E-6	5.04575749056067	22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	Adiponectin levels	1	1	1	1
rs4675644	9E-6	5.04575749056067	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs2383024	9E-6	5.04575749056067	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs10516809	9E-6	5.04575749056067	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs16856186	9E-6	5.04575749056067	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	0	1	1	1
rs10187654	9E-6	5.04575749056067	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	0	1	1	1
rs7027930	9E-6	5.04575749056067	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs2623702	9E-6	5.04575749056067	22424883	Genome-wide association study of lung function decline in adults with and without asthma.	Pulmonary function decline	1	1	1	1
rs881827	9E-6	5.04575749056067	22286170	The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes.	Lymphocyte counts	1	1	1	1
rs2459210	9E-6	5.04575749056067	22443383	Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.	Hemostatic factors and hematological phenotypes	NA	NA	NA	NA
rs2071598	9E-6	5.04575749056067	22210626	Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.	Prion diseases	1	1	1	1
rs3743162	9E-6	5.04575749056067	22005931	Genome-wide association analysis of age-at-onset in Alzheimer's disease.	Alzheimer's disease (age of onset)	1	1	1	1
rs2086512	9E-6	5.04575749056067	21993531	Genome-wide association study does not reveal major genetic determinants for anti-cytomegalovirus antibody response.	Cytomegalovirus antibody response	1	1	1	1
rs17793829	9E-6	5.04575749056067	21993531	Genome-wide association study does not reveal major genetic determinants for anti-cytomegalovirus antibody response.	Cytomegalovirus antibody response	1	1	1	1
rs10805321	9E-6	5.04575749056067	21990027	The genetics of antipsychotic induced tremors: a genome-wide pathway analysis on the STEP-BD SCP sample.	Response to antipsychotic therapy (extrapyramidal side effects)	1	1	1	1
rs2544527	9E-6	5.04575749056067	21946350	Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.	Pulmonary function	1	1	1	1
rs545610	9E-6	5.04575749056067	21940522	Genome-wide association scan for childhood caries implicates novel genes.	Dental caries	0	0	0	0
rs7827290	9E-6	5.04575749056067	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	0	1	1	1
rs6550435	9E-6	5.04575749056067	21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.	Bipolar disorder	0	0	1	1
rs732505	9E-6	5.04575749056067	21810271	Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.	vWF and FVIII levels	1	1	1	1
rs2367725	9E-6	5.04575749056067	21782286	A genome-wide association study of aging.	Aging (time to event)	0	1	1	1
rs2289700	9E-6	5.04575749056067	21771265	Genome-wide association study on bipolar disorder in the Bulgarian population.	Bipolar disorder	0	1	1	1
rs6983267	9E-6	5.04575749056067	21743057	Genome-wide association study identifies new prostate cancer susceptibility loci.	Prostate cancer	0	0	1	1
rs7747960	9E-6	5.04575749056067	21738484	Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes.	Bipolar disorder	0	0	1	1
rs4770394	9E-6	5.04575749056067	21738484	Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes.	Bipolar disorder	1	1	1	1
rs1038094	9E-6	5.04575749056067	21738484	Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes.	Bipolar disorder	1	1	1	1
rs2793086	9E-6	5.04575749056067	21659360	Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial.	Response to antineoplastic agents	1	1	1	1
rs1015164	9E-6	5.04575749056067	21502085	Genome-wide association study implicates PARD3B-based AIDS restriction.	AIDS progression	0	0	0	0
rs6716455	9E-6	5.04575749056067	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (alcohol dependence factor score)	0	1	0	0
rs195204	9E-6	5.04575749056067	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (heaviness of drinking)	1	1	1	1
rs1380131	9E-6	5.04575749056067	21529783	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	Alcoholism (heaviness of drinking)	1	1	1	1
rs7117404	9E-6	5.04575749056067	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	1	1	1	1
rs11039571	9E-6	5.04575749056067	21502573	Genetic predictors of fibrin D-dimer levels in healthy adults.	D-dimer levels	0	1	1	1
rs1073203	9E-6	5.04575749056067	21441570	Genome-wide meta-analysis for severe diabetic retinopathy.	Diabetic retinopathy 	1	1	1	1
rs10982256	9E-6	5.04575749056067	21254220	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Bipolar disorder	1	1	1	1
rs2207418	9E-6	5.04575749056067	21348951	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Cardiac hypertrophy	0	1	1	1
rs7283316	9E-6	5.04575749056067	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs1884136	9E-6	5.04575749056067	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs9985399	9E-6	5.04575749056067	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	1	1	1	1
rs11542478	9E-6	5.04575749056067	21130836	Whole genome association scan for genetic polymorphisms influencing information processing speed.	Information processing speed	0	1	1	1
rs12279261	9E-6	5.04575749056067	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Entorhinal cortical thickness	NA	NA	NA	NA
rs3905000	9E-6	5.04575749056067	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	MRI atrophy measures	0	1	1	1
rs10937470	9E-6	5.04575749056067	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	1	1	1	1
rs7805803	9E-6	5.04575749056067	21116278	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	Total ventricular volume	1	1	1	1
rs830998	9E-6	5.04575749056067	21079607	A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.	Anorexia nervosa	1	1	1	1
rs6782029	9E-6	5.04575749056067	21079607	A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.	Anorexia nervosa	1	1	1	1
rs1371867	9E-6	5.04575749056067	21041692	Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science.	Atrioventricular conduction	1	1	1	1
rs6811556	9E-6	5.04575749056067	20848476	Genetic predictors of medically refractory ulcerative colitis.	Ulcerative colitis	1	1	1	1
rs4799088	9E-6	5.04575749056067	20801717	Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.	Amyotrophic lateral sclerosis	1	1	1	1
rs6986718	9E-6	5.04575749056067	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs1395103	9E-6	5.04575749056067	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs10508558	9E-6	5.04575749056067	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs11168351	9E-6	5.04575749056067	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs28890483	9E-6	5.04575749056067	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs4822752	9E-6	5.04575749056067	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	0	1	1	1
rs6561750	9E-6	5.04575749056067	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs7465272	9E-6	5.04575749056067	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs9561428	9E-6	5.04575749056067	20889312	A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.	Bipolar disorder and schizophrenia	1	1	1	1
rs13387042	9E-6	5.04575749056067	20872241	A combined analysis of genome-wide association studies in breast cancer.	Breast cancer	0	0	1	1
rs8007846	9E-6	5.04575749056067	20802204	Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis.	Multiple sclerosis--Brain Glutamate Levels	0	1	1	1
rs10744304	9E-6	5.04575749056067	20800221	Genome-wide association scan of trait depression.	Depression (quantitative trait)	NA	NA	NA	NA
rs2017305	9E-6	5.04575749056067	20800221	Genome-wide association scan of trait depression.	Depression (quantitative trait)	0	1	1	1
rs838705	9E-6	5.04575749056067	20705733	Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.	Calcium levels	0	1	1	1
rs1305088	9E-6	5.04575749056067	20708005	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	Non-alcoholic fatty liver disease histology (other)	1	1	1	1
rs7029145	9E-6	5.04575749056067	20694011	Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.	Immunoglobulin A 	1	1	1	1
rs10176705	9E-6	5.04575749056067	20691247	A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality.	Personality dimensions	0	1	1	1
rs7852296	9E-6	5.04575749056067	20691247	A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality.	Personality dimensions	0	1	1	1
rs17478107	9E-6	5.04575749056067	20707712	A genome-wide association study of self-rated health.	Self-rated health	1	1	1	1
rs1799810	9E-6	5.04575749056067	20707712	A genome-wide association study of self-rated health.	Self-rated health	0	0	0	0
rs9548119	9E-6	5.04575749056067	20707712	A genome-wide association study of self-rated health.	Self-rated health	1	1	1	1
rs10941694	9E-6	5.04575749056067	20686651	Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases.	Chronic kidney disease and serum creatinine levels	1	1	1	1
rs2475335	9E-6	5.04575749056067	20522523	Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.	Partial epilepsies	1	1	1	1
rs13074924	9E-6	5.04575749056067	20516156	Genome-wide association study of major recurrent depression in the U.K. population.	Major depressive disorder	1	1	1	1
rs4709845	9E-6	5.04575749056067	20516156	Genome-wide association study of major recurrent depression in the U.K. population.	Major depressive disorder	1	1	1	1
rs10487524	9E-6	5.04575749056067	20732626	Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	1	1	1	1
rs17159640	9E-6	5.04575749056067	20400778	Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.	Mortality among heart failure patients	0	1	1	1
rs10483727	9E-6	5.04575749056067	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (rim)	0	1	1	1
rs735854	9E-6	5.04575749056067	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (rim)	1	1	1	1
rs2500535	9E-6	5.04575749056067	20360315	Genome-wide pharmacogenetics of antidepressant response in the GENDEP project.	Response to antidepressants	0	0	0	0
rs10270805	9E-6	5.04575749056067	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs16839962	9E-6	5.04575749056067	20339536	Genome-wide association of lipid-lowering response to statins in combined study populations.	Response to statin therapy	1	1	1	1
rs2224865	9E-6	5.04575749056067	20208534	Common variants at 5q22 associate with pediatric eosinophilic esophagitis.	Eosinophilic esophagitis (pediatric)	1	1	1	1
rs1891498	9E-6	5.04575749056067	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs7659062	9E-6	5.04575749056067	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	0	0	0	0
rs7662358	9E-6	5.04575749056067	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	0	0	0	0
rs13169113	9E-6	5.04575749056067	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs2289577	9E-6	5.04575749056067	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs1124769	9E-6	5.04575749056067	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs6050267	9E-6	5.04575749056067	20125193	Common genetic variation and performance on standardized cognitive tests.	Cognitive performance	1	1	1	1
rs9572423	9E-6	5.04575749056067	20125088	Genome-wide association study of recurrent early-onset major depressive disorder.	Major depressive disorder	1	1	1	1
rs2834812	9E-6	5.04575749056067	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs10159302	9E-6	5.04575749056067	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs2637496	9E-6	5.04575749056067	20041166	Common genetic variation and the control of HIV-1 in humans.	HIV-1 control	1	1	1	1
rs17605562	9E-6	5.04575749056067	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	1	1	1	1
rs17316633	9E-6	5.04575749056067	19896111	Common variants in the trichohyalin gene are associated with straight hair in Europeans.	Hair morphology	0	1	1	1
rs10972341	9E-6	5.04575749056067	19851299	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	Weight	1	1	1	1
rs7577851	9E-6	5.04575749056067	19772629	Genomewide association study for onset age in Parkinson disease.	Parkinson's disease (age of onset)	1	1	1	1
rs12155172	9E-6	5.04575749056067	19767753	Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.	Prostate cancer	0	0	1	1
rs1556032	9E-6	5.04575749056067	19754311	Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03).	AIDS	0	1	1	1
rs10856240	9E-6	5.04575749056067	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	NA	NA	NA	NA
rs969962	9E-6	5.04575749056067	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs1324015	9E-6	5.04575749056067	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs4861096	9E-6	5.04575749056067	19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	Cognitive performance	1	1	1	1
rs10849033	9E-6	5.04575749056067	19684603	Germline genomic variants associated with childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs1879352	9E-6	5.04575749056067	19684603	Germline genomic variants associated with childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs563507	9E-6	5.04575749056067	19684603	Germline genomic variants associated with childhood acute lymphoblastic leukemia.	Acute lymphoblastic leukemia (childhood)	1	1	1	1
rs1364705	9E-6	5.04575749056067	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs6590322	9E-6	5.04575749056067	19668339	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	Hippocampal atrophy	1	1	1	1
rs10192369	9E-6	5.04575749056067	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs2823962	9E-6	5.04575749056067	19451621	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs1035050	9E-6	5.04575749056067	19416921	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.	Bipolar disorder	1	1	1	1
rs950063	9E-6	5.04575749056067	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	0	1	1	1
rs6444087	9E-6	5.04575749056067	19247474	Genome-wide and candidate gene association study of cigarette smoking behaviors.	Smoking behavior	0	1	1	1
rs12658202	9E-6	5.04575749056067	19260139	Genome-wide association study of anthropometric traits in Korcula Island, Croatia.	Anthropometric traits	NA	NA	NA	NA
rs7499892	9E-6	5.04575749056067	19260141	Genome-wide association study of biochemical traits in Korcula Island, Croatia.	Biochemical measures	0	1	1	1
rs7722022	9E-6	5.04575749056067	19165155	Genome-wide linkage and association analyses to identify genes influencing adiponectin levels: the GEMS Study.	Adiponectin levels	0	1	1	1
rs4730276	9E-6	5.04575749056067	19122664	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.	Ulcerative colitis	0	0	0	0
rs12044355	9E-6	5.04575749056067	19118814	Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease.	Alzheimer's disease	1	1	1	1
rs932316	9E-6	5.04575749056067	19084217	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.	Iron status biomarkers	0	0	0	0
rs10490823	9E-6	5.04575749056067	19079262	New sequence variants associated with bone mineral density.	Bone mineral density (hip)	0	0	1	1
rs17367118	9E-6	5.04575749056067	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	1	1	1	1
rs2290416	9E-6	5.04575749056067	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	0	1	1	1
rs272000	9E-6	5.04575749056067	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Attention deficit hyperactivity disorder	1	1	1	1
rs17658378	9E-6	5.04575749056067	18937294	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.	Attention deficit hyperactivity disorder (time to onset)	NA	NA	NA	NA
rs1202199	9E-6	5.04575749056067	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Hyperactive-impulsive symptoms	1	1	1	1
rs13353224	9E-6	5.04575749056067	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Hyperactive-impulsive symptoms	1	1	1	1
rs11786458	9E-6	5.04575749056067	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	1	1	1	1
rs13330107	9E-6	5.04575749056067	18821565	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	Inattentive symptoms	0	1	1	1
rs9491640	9E-6	5.04575749056067	19023125	A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype.	Brain imaging in schizophrenia (interaction)	1	1	1	1
rs1109670	9E-6	5.04575749056067	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis	1	1	1	1
rs337718	9E-6	5.04575749056067	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (severity)	1	1	1	1
rs7253363	9E-6	5.04575749056067	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Multiple sclerosis (severity)	1	1	1	1
rs11957313	9E-6	5.04575749056067	19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Normalized brain volume	1	1	1	1
rs2180233	9E-6	5.04575749056067	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs10797919	9E-6	5.04575749056067	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs2764980	9E-6	5.04575749056067	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs9512900	9E-6	5.04575749056067	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	1	1	1	1
rs12921846	9E-6	5.04575749056067	18951430	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	Attention deficit hyperactivity disorder and conduct disorder	0	1	1	1
rs4875598	9E-6	5.04575749056067	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Attention deficit hyperactivity disorder symptoms (interaction)	1	1	1	1
rs16880441	9E-6	5.04575749056067	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	1	1	1	1
rs17116334	9E-6	5.04575749056067	18846501	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	Conduct disorder (interaction)	1	1	1	1
rs17039212	9E-6	5.04575749056067	19165918	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.	Systemic lupus erythematosus	1	1	1	1
rs3825776	9E-6	5.04575749056067	18084291	Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs7580332	9E-6	5.04575749056067	18084291	Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	1	1	1	1
rs10501920	9E-6	5.04575749056067	17903304	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.	Atrial fibrillation	0	1	1	1
rs740363	9E-6	5.04575749056067	17903304	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.	Heart failure	1	1	1	1
rs2066219	9E-6	5.04575749056067	17903298	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	Diabetes related insulin traits	1	1	1	1
rs2722425	9E-6	5.04575749056067	17903298	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	Fasting plasma glucose	0	0	0	0
rs1350445	9E-6	5.04575749056067	17903303	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	Subclinical atherosclerosis traits (other)	1	1	1	1
rs1502050	9E-6	5.04575749056067	17903303	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	Subclinical atherosclerosis traits (other)	0	0	0	0
rs934299	9E-6	5.04575749056067	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Cognitive test performance	1	1	1	1
rs360929	9E-6	5.04575749056067	17903297	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Volumetric brain MRI	0	1	1	1
rs357394	9E-6	5.04575749056067	17903307	Framingham Heart Study genome-wide association: results for pulmonary function measures.	Pulmonary function	1	1	1	1
rs4591494	9E-6	5.04575749056067	17903294	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Factor VII	1	1	1	1
rs6601764	9E-6	5.04575749056067	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Crohn's disease	1	1	1	1
rs3816587	9E-6	5.04575749056067	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Rheumatoid arthritis	1	1	1	1
rs7659604	9E-6	5.04575749056067	17554300	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	Type 2 diabetes	1	1	1	1
rs6887695	9E-6	5.04575749056067	17554261	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.	Crohn's disease	0	0	1	1
rs981782	9E-6	5.04575749056067	17529967	Genome-wide association study identifies novel breast cancer susceptibility loci.	Breast cancer	0	1	1	1
rs783396	9E-6	5.04575749056067	17434096	A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.	Stroke	1	1	1	1
rs11099864	9E-6	5.04575749056067	17362836	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.	Amyotrophic lateral sclerosis	1	1	1	1
NR	NS	NA	23728906	A genome-wide association study of sleep habits and insomnia.	Sleep latency	NA	NA	NA	NA
rs12186641	7E-6	NA	23708191	Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.	Congenital heart disease	0	1	1	1
NR	NS	NA	23704207	Genome-wide association study of genetic predictors of overall survival for non-small cell lung cancer in never smokers.	Non-small cell lung cancer (survival)	NA	NA	NA	NA
NR	NS	NA	23668334	Genome scan study of prostate cancer in Arabs: identification of three genomic regions with multiple prostate cancer susceptibility loci in Tunisians.	Prostate cancer	NA	NA	NA	NA
NR	NS	NA	23661040	Genome-wide scan on total serum IgE levels identifies no common variants in a healthy Chinese male population.	IgE levels 	NA	NA	NA	NA
NR	NS	NA	23658558	Genome-wide association study of personality traits in the long life family study.	Personality dimensions	NA	NA	NA	NA
rs728996, rs2894788, rs6458777, rs4715233, rs9296661, rs1326589	5E-8	NA	23633212	Genome-wide association of single-nucleotide polymorphisms with weight loss outcomes after Roux-en-Y gastric bypass surgery.	Weight loss (gastric bypass surgery)	NA	NA	NA	NA
NR	NS	NA	23626673	Genetic variants associated with increased risk of malignant pleural mesothelioma: a genome-wide association study.	Malignant pleural mesothelioma	NA	NA	NA	NA
NR	NS	NA	23592221	Shared genetic factors for age at natural menopause in Iranian and European women.	Menopause (age at onset)	NA	NA	NA	NA
NR	NS	NA	23565138	First genome-wide association study on anxiety-related behaviours in childhood.	Anxiety	NA	NA	NA	NA
HLA-B*0702	8E-8	NA	23482656	Genome-wide association study of susceptibility loci for cervical cancer.	Cervical cancer	NA	NA	NA	NA
DRB1*1301-DQA1*0103-DQB1*0603	9E-10	NA	23482656	Genome-wide association study of susceptibility loci for cervical cancer.	Cervical cancer	NA	NA	NA	NA
DRB1*1501-DQB1*0602	4E-7	NA	23482656	Genome-wide association study of susceptibility loci for cervical cancer.	Cervical cancer	NA	NA	NA	NA
SNP_A-2171106	1E-16	NA	23536807	A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel Loci.	Age-related macular degeneration	NA	NA	NA	NA
SNP_A-1841655	1E-16	NA	23536807	A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel Loci.	Age-related macular degeneration	NA	NA	NA	NA
rs10917151, rs4654783, rs2235529	7E-9	NA	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	NA	NA	NA	NA
rs10917151, rs4654783, rs2235529	6E-6	NA	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	NA	NA	NA	NA
rs10917151, rs4654783, rs2235529, rs16826658, rs7521902	8E-7	NA	23472165	Genome-wide association study link novel loci to endometriosis.	Endometriosis	NA	NA	NA	NA
rs12043259, rs6747023, rs7589342, rs12995333, rs4851870, rs1465641, rs1465639, rs6741172, rs12995849, rs2163350, rs7589561, rs4851095, rs2377339, rs2163349	2E-11	NA	23533358	NCK2 is significantly associated with opiates addiction in African-origin men.	Addiction	NA	NA	NA	NA
rs1715	6E-7	NA	23453885	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	NA	NA	NA	NA
NR	NS	NA	23423446	A genome-wide association study to identify genetic susceptibility loci that modify ductal and lobular postmenopausal breast cancer risk associated with menopausal hormone therapy use: a two-stage design with replication.	Breast cancer (menopausal hormone therapy interaction)	NA	NA	NA	NA
Position 173336636	6E-7	NA	23419831	APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.	Alzheimer's disease biomarkers	NA	NA	NA	NA
rs24449894	2E-6	NA	23419831	APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.	Alzheimer's disease biomarkers	NA	NA	NA	NA
NR	NS	NA	23388002	Genetic associations with valvular calcification and aortic stenosis.	Mitral annular calcification	NA	NA	NA	NA
HLA-A*02:01	9E-10	NA	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	NA	NA	NA	NA
HLA-A*01:01	1E-8	NA	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	NA	NA	NA	NA
HLA-A*03:01	2E-6	NA	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	NA	NA	NA	NA
HLA-B*08:01	2E-20	NA	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	NA	NA	NA	NA
HLA-B*15:01	2E-10	NA	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	NA	NA	NA	NA
HLA-B*57:01	4E-7	NA	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	NA	NA	NA	NA
HLA-C*07:01	1E-18	NA	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	NA	NA	NA	NA
HLA-C*03:04	8E-8	NA	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	NA	NA	NA	NA
HLA-C*03:03	1E-6	NA	23417110	Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.	Beta-2 microglubulin plasma levels	NA	NA	NA	NA
NR	NS	NA	23392654	Genetic variation in PEAR1 is associated with platelet aggregation and cardiovascular outcomes.	Response to antiplatelet therapy	NA	NA	NA	NA
rs2270875, rs7832443	9E-6	NA	23374588	Pharmacogenomics in Alzheimer's disease: a genome-wide association study of response to cholinesterase inhibitors.	Response to cholinesterase inhibitors in Alzheimer's disease	NA	NA	NA	NA
rs17798800, rs492452	7E-6	NA	23374588	Pharmacogenomics in Alzheimer's disease: a genome-wide association study of response to cholinesterase inhibitors.	Response to cholinesterase inhibitors in Alzheimer's disease	NA	NA	NA	NA
NR	NS	NA	23337944	Opioid receptor mu 1 gene, fat intake and obesity in adolescence.	Fat intake	NA	NA	NA	NA
NR	NS	NA	23337848	A polymorphism in the protein kinase C gene PRKCB is associated with α2-adrenoceptor-mediated vasoconstriction.	Vascular constriction	NA	NA	NA	NA
rs1329424	NS	NA	23326517	Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.	Age-related macular degeneration	0	0	0	0
rs687289, rs8176704, rs8176749	2E-138	NA	23267103	Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.	Coagulation factor levels	NA	NA	NA	NA
rs687289, rs8176704, rs8176749	4E-98	NA	23267103	Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.	Coagulation factor levels	NA	NA	NA	NA
rs687289, rs8176704, rs8176749	7E-50	NA	23267103	Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.	Coagulation factor levels	NA	NA	NA	NA
rs1063856, rs1063857	6E-7	NA	23267103	Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.	Coagulation factor levels	NA	NA	NA	NA
NR	NS	NA	23263444	Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity.	Lipoprotein diameter	NA	NA	NA	NA
NR	NS	NA	23255317	Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathy.	Hypertrophic cardiomyopathy	NA	NA	NA	NA
rs74733271	5E-6	NA	23247143	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Cardiac Troponin-T levels	NA	NA	NA	NA
NR	NS	NA	23237013	Estimating the heritability of reporting stressful life events captured by common genetic variants.	Reporting of stressful life event	NA	NA	NA	NA
NR	NS	NA	23233654	Genome-wide association analysis of anti-TNF drug response in patients with rheumatoid arthritis.	Response to TNF-alpha inhibitors in rheumatoid arthritis	NA	NA	NA	NA
rs322458, rs17740066	6E-9	NA	23223146	A genome-wide association study in Caucasian women points out a putative role of the STXBP5L gene in facial photoaging.	Aging (facial)	NA	NA	NA	NA
rs322458, rs6782025	4E-9	NA	23223146	A genome-wide association study in Caucasian women points out a putative role of the STXBP5L gene in facial photoaging.	Aging (facial)	NA	NA	NA	NA
rs322458, rs6775899	1E-9	NA	23223146	A genome-wide association study in Caucasian women points out a putative role of the STXBP5L gene in facial photoaging.	Aging (facial)	NA	NA	NA	NA
rs12149070	8E-6	NA	23144326	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Chronic obstructive pulmonary disease-related biomarkers	NA	NA	NA	NA
NR	NS	NA	23114982	Genome-wide investigation of gene-environment interactions in colorectal cancer.	Colorectal cancer	NA	NA	NA	NA
rs2199936	2E-10	NA	23118302	Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.	Lipoprotein-associated phospholipase A2 activity change in response to statin therapy	NA	NA	NA	NA
NR	NS	NA	23133572	Genome-wide association study to identify the genetic determinants of otitis media susceptibility in childhood.	Otitis media	NA	NA	NA	NA
NR	NS	NA	23100282	Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study.	Response to statin therapy	NA	NA	NA	NA
rs2829459	3E-6	NA	23064961	GWAS of dental caries patterns in the permanent dentition.	Dental caries	NA	NA	NA	NA
NR	NS	NA	23054467	New single nucleotide polymorphisms associated with differences in platelets reactivity in patients with type 2 diabetes treated with acetylsalicylic acid: genome-wide association approach and pooled DNA strategy.	Platelet reactivity	NA	NA	NA	NA
NR	NS	NA	23010768	Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1.	Bipolar disorder (Negative mood delusions)	NA	NA	NA	NA
NR	NS	NA	22986903	Genome-wide study identifies two loci associated with lung function decline in mild to moderate COPD.	Chronic obstructive pulmonary disease	NA	NA	NA	NA
NR	NS	NA	23028347	A genome-wide association study identifies five loci influencing facial morphology in Europeans.	Facial morphology	NA	NA	NA	NA
NR	NS	NA	22981920	KCNIP4 as a candidate gene for personality disorders and adult ADHD.	Personality disorders	NA	NA	NA	NA
NR	NS	NA	22945461	Genome-wide association study reveals a complex genetic architecture underpinning-induced CYP3A4 enzyme activity.	CYP3A4 enzyme activity	NA	NA	NA	NA
NR	NS	NA	22935194	A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale.	Autism	NA	NA	NA	NA
rs41453448,rs1125777,rs12568010	2E-7	NA	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	NA	NA	NA	NA
rs1125777, rs12568010	2E-7	NA	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	NA	NA	NA	NA
rs17121983, rs7556462	4E-7	NA	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	NA	NA	NA	NA
rs7556462, rs4915737	4E-7	NA	22925353	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	Bipolar disorder	NA	NA	NA	NA
NR	NS	NA	22915352	Dissecting the genetic heterogeneity of depression through age at onset.	Depression (age of onset)	NA	NA	NA	NA
NR	NS	NA	22907730	Pharmacogenomics of selective serotonin reuptake inhibitor treatment for major depressive disorder: genome-wide associations and functional genomics.	Response to antidepressants	NA	NA	NA	NA
NR	NS	NA	22869035	A genome-wide association study of post-traumatic stress disorder identifies the retinoid-related orphan receptor alpha (RORA) gene as a significant risk locus.	Post-traumatic stress disorder	NA	NA	NA	NA
NR	NS	NA	22843789	A genome-wide association study identifies novel loci for paclitaxel-induced sensory peripheral neuropathy in CALGB 40101.	Paclitaxel-induced neuropathy	NA	NA	NA	NA
NR	NS	NA	22843499	Genome-wide meta-analysis of common variant differences between men and women.	Sex ratio at birth	NA	NA	NA	NA
NR	NS	NA	22828495	Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach.	Neural processing (facial expression)	NA	NA	NA	NA
NR	NS	NA	22911860	Genome wide assessment of young onset Parkinson's disease from Finland.	Parkinson's disease	NA	NA	NA	NA
rs5941160	2E-20	NA	22808956	Genetically distinct subsets within ANCA-associated vasculitis.	Antineutrophil cytoplasmic antibody-associated vasculitis 	NA	NA	NA	NA
NR	NS	NA	22785395	Identification of a late onset Alzheimer's disease candidate risk variant at 9q21.33 in Polish patients.	Alzheimer's disease	NA	NA	NA	NA
NR	NS	NA	22794196	Genome-wide association study for ovarian cancer susceptibility using pooled DNA.	Ovarian cancer	NA	NA	NA	NA
chr22:40779964	5E-7	NA	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	NA	NA	NA	NA
chr22:45895495	7E-6	NA	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	NA	NA	NA	NA
chr6:50202617	5E-6	NA	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	NA	NA	NA	NA
chr6:67596834	7E-6	NA	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	NA	NA	NA	NA
chr3:130947635	5E-7	NA	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	NA	NA	NA	NA
chr4:187239569	6E-6	NA	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	NA	NA	NA	NA
chr3:116704634	8E-6	NA	22747683	Genetic variants associated with breast size also influence breast cancer risk.	Breast size	NA	NA	NA	NA
NR	NS	NA	22701019	A genome-wide association study identifies KNG1 as a genetic determinant of plasma factor XI Level and activated partial thromboplastin time.	Factor XI	NA	NA	NA	NA
NR	NS	NA	22692763	Assessment of gene-by-sex interaction effect on bone mineral density.	Bone mineral density (interaction)	NA	NA	NA	NA
NR	NS	NA	22694930	Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases.	Asthma	NA	NA	NA	NA
NR	NS	NA	22665904	A replication study and genome-wide scan of single-nucleotide polymorphisms associated with pancreatic cancer risk and overall survival.	Pancreatic cancer	NA	NA	NA	NA
NR	NS	NA	22661486	Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia.	Central corneal thickness	NA	NA	NA	NA
NR	NS	NA	22628180	Genome-wide association uncovers shared genetic effects among personality traits and mood states.	Personality dimensions	NA	NA	NA	NA
NR	NS	NA	22633400	Genome-wide association study identifies candidate genes for male fertility traits in humans.	Male fertility	NA	NA	NA	NA
APOE	2E-33	NA	22745009	Multiple loci influencing hippocampal degeneration identified by genome scan.	Hippocampal atrophy	NA	NA	NA	NA
APOE	1E-7	NA	22745009	Multiple loci influencing hippocampal degeneration identified by genome scan.	Hippocampal atrophy	NA	NA	NA	NA
ch2:211694960	7E-6	NA	22561531	Genome-wide association study to identify genetic determinants of severe asthma.	Asthma	NA	NA	NA	NA
NR	NS	NA	22605921	Genome-wide association study of primary open angle glaucoma risk and quantitative traits.	Glaucoma (primary open-angle)	NA	NA	NA	NA
NR	NS	NA	22526605	Genetic association of zinc transporter 8 (ZnT8) autoantibodies in type 1 diabetes cases.	Type 1 diabetes autoantibodies	NA	NA	NA	NA
GA009635	7E-7	NA	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	NA	NA	NA	NA
SNP2-179127489	4E-7	NA	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	NA	NA	NA	NA
SNP3-186373264	2E-7	NA	22491018	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Response to tocilizumab in rheumatoid arthritis	NA	NA	NA	NA
NR	NS	NA	22466613	Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis.	Cystic fibrosis (meconium ileus) 	NA	NA	NA	NA
NR	NS	NA	22437316	Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris.	Pemphigus vulgaris	NA	NA	NA	NA
rs7081208, rs2446581, rs17314229	1E-10	NA	22430674	Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease.	Alzheimer's disease	NA	NA	NA	NA
H1H2	8E-52	NA	22438815	Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.	Parkinson's disease	NA	NA	NA	NA
NR	NS	NA	22432041	Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene.	Preeclampsia	NA	NA	NA	NA
NR	NS	NA	22613542	ANKRD7 and CYTL1 are novel risk genes for alcohol drinking behavior.	Drinking behavior	NA	NA	NA	NA
rs6043979, rs932541, rs6044001, rs6044003	1E-8	NA	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	NA	NA	NA	NA
rs3758171, rs1329573, rs3824344, rs7020413	4E-8	NA	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	NA	NA	NA	NA
rs3815908, rs2303690, rs3936340, rs2560966	3E-8	NA	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	NA	NA	NA	NA
rs2540051, rs7563911, rs7589014, rs2348114	6E-8	NA	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	NA	NA	NA	NA
rs11703808, rs761746, rs12627933, rs9621305	7E-8	NA	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	NA	NA	NA	NA
rs34312136, rs35079168, rs4501664, rs11102986	8E-8	NA	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	NA	NA	NA	NA
rs16835742, rs7533254, rs528059, rs544991	8E-8	NA	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	NA	NA	NA	NA
rs10834449, rs2716458, rs12798374, rs1021261	8E-8	NA	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	NA	NA	NA	NA
rs10262915, rs6465411, rs13221576, rs4729127	9E-8	NA	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	NA	NA	NA	NA
rs1987511, rs7475343, rs9423406, rs7896729	9E-8	NA	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	NA	NA	NA	NA
rs1908039, rs11099040, rs13113376, rs1908038	9E-8	NA	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	NA	NA	NA	NA
rs6781149, rs17584516, rs4629318, rs11713158	1E-7	NA	22449649	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	Intelligence	NA	NA	NA	NA
NR	NS	NA	22377092	ANAPC1 and SLCO3A1 are associated with nicotine dependence: meta-analysis of genome-wide association studies.	Nicotine dependence	NA	NA	NA	NA
NR	NS	NA	22362865	A genome-wide study on the perception of the odorants androstenone and galaxolide.	Odorant perception	NA	NA	NA	NA
NR	NS	NA	22333899	Genome-wide analysis of epistasis in body mass index using multiple human populations.	Body mass index	NA	NA	NA	NA
NR	NS	NA	22310351	Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration.	Fluorouracil treatment response in colorectal cancer	NA	NA	NA	NA
NR	NS	NA	22420046	Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.	Attention deficit hyperactivity disorder	NA	NA	NA	NA
NR	NS	NA	22295056	Genome wide association identifies PPFIA1 as a candidate gene for acute lung injury risk following major trauma.	Acute lung injury	NA	NA	NA	NA
NR	NS	NA	22279548	Genetic signatures of exceptional longevity in humans.	Longevity	NA	NA	NA	NA
rs17310467, rs6088735, rs6060278, rs867186	4E-34	NA	22443383	Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.	Hemostatic factors and hematological phenotypes	NA	NA	NA	NA
NA	NA	NA	NA	NA	NA	NA	NA	NA	NA
NR	7E-16	NA	22245343	A large scale multivariate parallel ICA method reveals novel imaging-genetic relationships for Alzheimer's disease in the ADNI cohort.	Alzheimer's disease	NA	NA	NA	NA
NR	4E-9	NA	22245343	A large scale multivariate parallel ICA method reveals novel imaging-genetic relationships for Alzheimer's disease in the ADNI cohort.	Alzheimer's disease	NA	NA	NA	NA
NR	NS	NA	22156575	KCTD8 gene and brain growth in adverse intrauterine environment: a genome-wide association study.	Brain development	NA	NA	NA	NA
NR	NS	NA	22140272	A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation.	Testicular dysgenesis syndrome 	NA	NA	NA	NA
NR	NS	NA	22105264	Identification of six loci associated with pelvic organ prolapse using genome-wide association analysis.	Pelvic organ prolapse	NA	NA	NA	NA
NR	NS	NA	22116812	Genome-wide association study of vascular dementia.	Vascular dementia	NA	NA	NA	NA
NR	NS	NA	22105620	A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene.	Memory performance	NA	NA	NA	NA
rs204999,rs9268528,rs9268542,rs6903608,rs2858870	2E-7	NA	22086417	A genome-wide meta-analysis of nodular sclerosing Hodgkin lymphoma identifies risk loci at 6p21.32.	Nodular sclerosis Hodgkin lymphoma	NA	NA	NA	NA
rs204999, rs9268528, rs9268542, rs6903608, rs2858870	8E-18	NA	22086417	A genome-wide meta-analysis of nodular sclerosing Hodgkin lymphoma identifies risk loci at 6p21.32.	Nodular sclerosis Hodgkin lymphoma	NA	NA	NA	NA
NR	NS	NA	22072270	Genome-wide association study identifies 5q21 and 9p24.1 (KDM4C) loci associated with alcohol withdrawal symptoms.	Alcohol withdrawal symptoms	NA	NA	NA	NA
NR	NS	NA	22051697	Genome-wide association study reveals class I MHC-restricted T cell-associated molecule gene (CRTAM) variants interact with vitamin D levels to affect asthma exacerbations.	Asthma	NA	NA	NA	NA
NR	NS	NA	22295569	[Genome-wide association study of bronchial asthma in the Volga-Ural region of Russia].	Asthma	NA	NA	NA	NA
NR	NS	NA	22010049	Loci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations.	Gamma gluatamyl transferase levels (interaction with age)	NA	NA	NA	NA
NR	NS	NA	22027810	Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata.	Alopecia areata	NA	NA	NA	NA
NR	NS	NA	22030708	Genome-wide association study of antidepressant treatment-emergent suicidal ideation.	Suicidal ideation	NA	NA	NA	NA
NR	NS	NA	22029572	Recent methods for polygenic analysis of genome-wide data implicate an important effect of common variants on cardiovascular disease risk.	Cardiovascular disease risk factors	NA	NA	NA	NA
NR	NS	NA	22003120	Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus.	Corneal structure	NA	NA	NA	NA
NR	NS	NA	21996601	Genome-wide association studies for bivariate sparse longitudinal data.	Blood pressure	NA	NA	NA	NA
NR	NS	NA	21977987	Replication of LDL GWAs hits in PROSPER/PHASE as validation for future (pharmaco)genetic analyses.	LDL cholesterol	NA	NA	NA	NA
NR	NS	NA	21961650	Evidence for association of an ACCN1 gene variant with response to lithium treatment in Sardinian patients with bipolar disorder.	Response to lithium treatment in bipolar disorder	NA	NA	NA	NA
NR	NS	NA	21980348	Genome-wide assessment for genetic variants associated with ventricular dysfunction after primary coronary artery bypass graft surgery.	Postoperative ventricular dysfunction 	NA	NA	NA	NA
NR	NS	NA	21991891	Genomewide association between GLCCI1 and response to glucocorticoid therapy in asthma.	Asthma treatment response	NA	NA	NA	NA
rs2437258	3E-10	NA	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	NA	NA	NA	NA
rs2199936	2E-17	NA	21943158	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.	Cardiovascular disease risk factors	NA	NA	NA	NA
NR	NS	NA	21940970	Siblings with ischemic stroke study: results of a genome-wide scan for stroke loci.	Stroke	NA	NA	NA	NA
NR	NS	NA	21912186	Convergent genomic studies identify association of GRIK2 and NPAS2 with chronic fatigue syndrome.	Chronic fatigue syndrome	NA	NA	NA	NA
NR	NS	NA	21886828	Characterisation of genome-wide association epistasis signals for serum uric acid in human population isolates.	Uric acid levels	NA	NA	NA	NA
NR	NS	NA	21876681	Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee.	Parkinson's disease (interaction with coffee consumption)	NA	NA	NA	NA
DRB*15:01	1E-132	NA	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	NA	NA	NA	NA
DRB*13:03	1E-11	NA	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	NA	NA	NA	NA
DRB*03:01	4E-10	NA	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	NA	NA	NA	NA
A*02:01	9E-23	NA	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	NA	NA	NA	NA
DRB*08:01	2E-7	NA	21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Multiple sclerosis	NA	NA	NA	NA
NR	NS	NA	21826061	Genome-wide association studies establish that human intelligence is highly heritable and polygenic.	Intelligence	NA	NA	NA	NA
NR	NS	NA	21826682	Association of common variants in the human eyes shut ortholog (EYS) with statin-induced myopathy: evidence for additional functions of EYS.	Response to statin therapy	NA	NA	NA	NA
NR	NS	NA	21795503	Identification of new schizophrenia susceptibility loci in an ethnically homogeneous, family-based, Arab-Israeli sample.	Schizophrenia	NA	NA	NA	NA
NR	NS	NA	21777205	Evidence for age as a modifier of genetic associations for lipid levels.	Lipid traits	NA	NA	NA	NA
NR	NS	NA	21811574	Genome-wide association scan in HIV-1-infected individuals identifying variants influencing disease course.	HIV-1 progression	NA	NA	NA	NA
NR	NS	NA	21752600	Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia.	Schizophrenia	NA	NA	NA	NA
NR	NS	NA	21747397	Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe.	Schizophrenia	NA	NA	NA	NA
NR	NS	NA	21750702	Genomewide association scan of suicidal thoughts and behaviour in major depression.	Suicidal ideation	NA	NA	NA	NA
NR	NS	NA	22303337	Pathway-Wide Association Study Implicates Multiple Sterol Transport and Metabolism Genes in HDL Cholesterol Regulation.	HDL cholesterol	NA	NA	NA	NA
NR	NS	NA	21694509	Genome-wide Association study using pooled DNA to identify candidate markers mediating susceptibility to postoperative nausea and vomiting.	Postoperative nausea and vomiting 	NA	NA	NA	NA
NR	NS	NA	21705454	Platinum sensitivity-related germline polymorphism discovered via a cell-based approach and analysis of its association with outcome in ovarian cancer patients.	Response to platinum-based agents	NA	NA	NA	NA
i4000416	5E-21	NA	21738487	Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.	Parkinson's disease	NA	NA	NA	NA
NR	NS	NA	21696813	Identification of ATPAF1 as a novel candidate gene for asthma in children.	Asthma	NA	NA	NA	NA
NR	NS	NA	21665988	Genome-wide significance and replication of the chromosome 12p11.22 locus near the PTHLH gene for peripartum cardiomyopathy.	Peripartum cardiomyopathy	NA	NA	NA	NA
NR	NS	NA	21694764	Educational attainment: a genome wide association study in 9538 Australians.	Educational attainment	NA	NA	NA	NA
rs12091564, rs10218795	2E-7	NA	21626137	Two-marker association tests yield new disease associations for coronary artery disease and hypertension.	Coronary heart disease	NA	NA	NA	NA
rs11924705, rs6789378	4E-14	NA	21626137	Two-marker association tests yield new disease associations for coronary artery disease and hypertension.	Coronary heart disease	NA	NA	NA	NA
rs7697839, rs7673097	2E-11	NA	21626137	Two-marker association tests yield new disease associations for coronary artery disease and hypertension.	Coronary heart disease	NA	NA	NA	NA
rs1333048, rs1333049	7E-14	NA	21626137	Two-marker association tests yield new disease associations for coronary artery disease and hypertension.	Coronary heart disease	NA	NA	NA	NA
rs1165668, rs1165669	3E-9	NA	21626137	Two-marker association tests yield new disease associations for coronary artery disease and hypertension.	Coronary heart disease	NA	NA	NA	NA
rs10496288, rs10496289	2E-9	NA	21626137	Two-marker association tests yield new disease associations for coronary artery disease and hypertension.	Hypertension	NA	NA	NA	NA
rs13420028, rs10188442	1E-10	NA	21626137	Two-marker association tests yield new disease associations for coronary artery disease and hypertension.	Hypertension	NA	NA	NA	NA
rs7735940, rs12522034	5E-13	NA	21626137	Two-marker association tests yield new disease associations for coronary artery disease and hypertension.	Hypertension	NA	NA	NA	NA
rs6452524, rs6887846	2E-7	NA	21626137	Two-marker association tests yield new disease associations for coronary artery disease and hypertension.	Hypertension	NA	NA	NA	NA
rs3798440, rs9350602	3E-10	NA	21626137	Two-marker association tests yield new disease associations for coronary artery disease and hypertension.	Hypertension	NA	NA	NA	NA
rs2469997, rs6469823	3E-16	NA	21626137	Two-marker association tests yield new disease associations for coronary artery disease and hypertension.	Hypertension	NA	NA	NA	NA
rs7827545, rs1372662	2E-44	NA	21626137	Two-marker association tests yield new disease associations for coronary artery disease and hypertension.	Hypertension	NA	NA	NA	NA
rs7960483, rs10785581	1E-7	NA	21626137	Two-marker association tests yield new disease associations for coronary artery disease and hypertension.	Hypertension	NA	NA	NA	NA
rs200752, rs200759	7E-9	NA	21626137	Two-marker association tests yield new disease associations for coronary artery disease and hypertension.	Hypertension	NA	NA	NA	NA
NR	NS	NA	21611967	Identification of homogeneous genetic architecture of multiple genetically correlated traits by block clustering of genome-wide associations.	Fracture-related traits	NA	NA	NA	NA
NR	NS	NA	21540310	A genome-wide association study reveals evidence of association with sarcoidosis at 6p12.1.	Sarcoidosis	NA	NA	NA	NA
NR	NS	NA	21497890	Genome-wide association identifies diverse causes of common variable immunodeficiency.	Common variable immunodeficiency	NA	NA	NA	NA
NR	NS	NA	21467234	Genome-wide association study identifies a genetic variant associated with risk for more aggressive prostate cancer.	Prostate cancer	NA	NA	NA	NA
rs17129789	9E-20	NA	21399635	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.	Primary biliary cirrhosis	NA	NA	NA	NA
NR	NS	NA	21378987	A rare variant in MYH6 is associated with high risk of sick sinus syndrome.	Sick sinus syndrome	NA	NA	NA	NA
NR	NS	NA	21357381	Genotype-environment interactions in microsatellite stable/microsatellite instability-low colorectal cancer: results from a genome-wide association study.	Colorectal cancer	NA	NA	NA	NA
NR	NS	NA	21359210	Pooled genome-wide analysis to identify novel risk loci for pediatric allergic asthma.	Asthma (childhood onset)	NA	NA	NA	NA
NR	NS	NA	21316860	Genetics of cortisol secretion and depressive symptoms: a candidate gene and genome wide association approach.	Cortisol secretion	NA	NA	NA	NA
NR	NS	NA	21497773	Germline polymorphisms discovered via a cell-based, genome-wide approach predict platinum response in head and neck cancers.	Response to platinum-based chemotherapy in head and neck cancers	NA	NA	NA	NA
NR	2E-14	NA	21292315	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.	Parkinson's disease	NA	NA	NA	NA
NR	NS	NA	21245432	HLA-DQA1*02:01 is a major risk factor for lapatinib-induced hepatotoxicity in women with advanced breast cancer.	Lapatinib-induced hepatotoxicity	NA	NA	NA	NA
NR	NS	NA	21283782	Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasis.	Nephrolithiasis	NA	NA	NA	NA
NR	NS	NA	21248740	Genome-wide association study confirms extant PD risk loci among the Dutch.	Parkinson's disease	NA	NA	NA	NA
NR	NS	NA	21242121	Multiple genetic loci modulate lung adenocarcinoma clinical staging.	Lung adenocarcinoma (clinical stage)	NA	NA	NA	NA
NR	NS	NA	21221126	Genome-wide association study of serious blistering skin rash caused by drugs.	Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS-TEN)	NA	NA	NA	NA
NR	NS	NA	21211648	Gene-environment interaction for childhood asthma and exposure to farming in Central Europe.	Asthma	NA	NA	NA	NA
NR	NS	NA	21183627	Genomic predictors of the maximal O₂ uptake response to standardized exercise training programs.	Maximal oxygen uptake response	NA	NA	NA	NA
NR	NS	NA	21177295	Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study.	Osteoarthritis	NA	NA	NA	NA
NR	NS	NA	21197116	Genome-wide association analyses of genetic, phenotypic, and environmental risks in the age-related eye disease study.	Age-related macular degeneration	NA	NA	NA	NA
NR	NS	NA	21130132	Genome-wide association study of blood pressure response to methylphenidate treatment of attention-deficit/hyperactivity disorder.	Response to methylphenidate treatment	NA	NA	NA	NA
NR	NS	NA	21098978	Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data.	Alzheimer's disease	NA	NA	NA	NA
NR	NS	NA	21094521	A genome-wide association study to identify genetic determinants of atopy in subjects from the United Kingdom.	Atopy	NA	NA	NA	NA
NR	NS	NA	21062454	A genome-wide association scan on estrogen receptor-negative breast cancer.	Breast cancer	NA	NA	NA	NA
NR	NS	NA	21061259	Genome-wide association study of genetic predictors of anti-tumor necrosis factor treatment efficacy in rheumatoid arthritis identifies associations with polymorphisms at seven loci.	Response to TNF antagonist treatment	NA	NA	NA	NA
NR	NS	NA	20978177	Genome-wide association study of prostate cancer mortality.	Prostate cancer mortality	NA	NA	NA	NA
NR	5E-31	NA	20972438	A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.	Bladder cancer	NA	NA	NA	NA
rs458017,rs465969	2E-16	NA	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	NA	NA	NA	NA
rs2235617,rs495337	2E-6	NA	20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Psoriasis	NA	NA	NA	NA
NR	NS	NA	20920776	PDE11A associations with asthma: results of a genome-wide association scan.	Asthma	NA	NA	NA	NA
rs3849942,rs10122902	8E-10	NA	20801717	Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.	Amyotrophic lateral sclerosis	NA	NA	NA	NA
rs3849942,rs10122902	5E-11	NA	20801717	Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.	Amyotrophic lateral sclerosis	NA	NA	NA	NA
rs2199936	1E-75	NA	20884846	Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.	Urate levels	NA	NA	NA	NA
rs2199936	3E-23	NA	20884846	Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.	Urate levels	NA	NA	NA	NA
NR	NS	NA	20826269	A locus on chromosome 1p36 is associated with thyrotropin and thyroid function as identified by genome-wide association study.	Thyroid function	NA	NA	NA	NA
NR	NS	NA	20808326	Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome.	Pseudoexfoliation syndrome	NA	NA	NA	NA
NR	NS	NA	20698975	Asthma-susceptibility variants identified using probands in case-control and family-based analyses.	Asthma	NA	NA	NA	NA
NR	NS	NA	20732627	Case-control genome-wide association study of attention-deficit/hyperactivity disorder.	Attention deficit hyperactivity disorder	NA	NA	NA	NA
NR	NS	NA	20602913	IRF4 variants have age-specific effects on nevus count and predispose to melanoma.	Nevus count	NA	NA	NA	NA
NR	NS	NA	20622880	Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction.	Ventricular fibrillation	NA	NA	NA	NA
NR	NS	NA	20610541	Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.	Colorectal cancer	NA	NA	NA	NA
NR	NS	NA	20558996	Pilot Study on Schizophrenia in Sardinia.	Schizophrenia	NA	NA	NA	NA
NR	NS	NA	20528957	A genome-wide association study of bipolar disorder and comorbid migraine.	Migraine in bipolar disorder	NA	NA	NA	NA
NR	NS	NA	20484958	Pooling-based genome-wide association study implicates gamma-glutamyltransferase 1 (GGT1) gene in pancreatic carcinogenesis.	Pancreatic cancer	NA	NA	NA	NA
NR	NS	NA	20451256	A genome-wide association study of bipolar disorder in Norwegian individuals, followed by replication in Icelandic sample.	Bipolar disorder	NA	NA	NA	NA
rs3829251,rs11234027	3E-9	NA	20418485	Genome-wide association study of circulating vitamin D levels.	Vitamin D levels	NA	NA	NA	NA
rs2060793,rs1993116	3E-17	NA	20418485	Genome-wide association study of circulating vitamin D levels.	Vitamin D levels	NA	NA	NA	NA
rs9692809	8E-6	NA	20395239	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	Optic disc size (cup)	NA	NA	NA	NA
NR	NS	NA	20370913	Genome-wide association analysis of total cholesterol and high-density lipoprotein cholesterol levels using the Framingham heart study data.	Cholesterol	NA	NA	NA	NA
NR	NS	NA	20360844	Genome-wide association study identifies GPC5 as a novel genetic locus protective against sudden cardiac arrest.	Sudden cardiac arrest	NA	NA	NA	NA
NR	NS	NA	20332263	A genome-wide association study of prognosis in breast cancer.	Breast cancer (prognosis)	NA	NA	NA	NA
NR	NS	NA	20306291	A three-stage genome-wide association study of general cognitive ability: hunting the small effects.	Cognitive ability	NA	NA	NA	NA
NR	NS	NA	20222955	A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level.	Creatinine levels	NA	NA	NA	NA
NR	NS	NA	20235792	Genome-wide association for smoking cessation success: participants in the Patch in Practice trial of nicotine replacement.	Smoking cessation	NA	NA	NA	NA
NR	NS	NA	20164292	Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women.	Bone mineral density	NA	NA	NA	NA
NR	NS	NA	20154673	Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.	Frontotemporal lobar degeneration	NA	NA	NA	NA
rs10932886	E	NA	20100581	Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort.	Brain imaging	1	1	1	1
rs429358	NS	NA	20100581	Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort.	Brain imaging	0	1	1	1
rs7610017	NS	NA	20100581	Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort.	Brain imaging	1	1	1	1
rs6463843	NS	NA	20100581	Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort.	Brain imaging	1	1	1	1
rs2075650	NS	NA	20100581	Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort.	Brain imaging	0	0	0	0
rs16912145	NS	NA	20100581	Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort.	Brain imaging	0	1	1	1
rs12531488	NS	NA	20100581	Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort.	Brain imaging	1	1	1	1
rs7526034	NS	NA	20100581	Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort.	Brain imaging	0	1	1	1
rs7647307	NS	NA	20100581	Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort.	Brain imaging	1	1	1	1
rs4692256	E	NA	20100581	Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort.	Brain imaging	1	1	1	1
NR	NS	NA	20044523	Genome-wide association studies of MRI-defined brain infarcts: meta-analysis from the CHARGE Consortium.	Subclinical brain infarct	NA	NA	NA	NA
NR	NS	NA	20038948	A genome-wide survey of human short-term memory.	Memory (short-term)	NA	NA	NA	NA
NR	NS	NA	20012890	A genome-wide association study of social and non-social autistic-like traits in the general population using pooled DNA, 500 K SNP microarrays and both community and diagnosed autism replication samples.	Social and non-social autistic-like traits	NA	NA	NA	NA
NR	NS	NA	20175129	Genome-wide association study for femoral neck bone geometry.	Femoral neck bone geometry	NA	NA	NA	NA
NR	NS	NA	19944697	Genome-wide association analysis in primary sclerosing cholangitis.	Primary sclerosing cholangitis	NA	NA	NA	NA
NR	NS	NA	20039944	A genome-wide association study identifies multiple loci associated with mathematics ability and disability.	Mathematical ability	NA	NA	NA	NA
NR	NS	NA	19929986	Genome-wide SNP genotyping study using pooled DNA to identify candidate markers mediating susceptibility to end-stage renal disease attributed to Type 1 diabetes.	End-stage renal disease	NA	NA	NA	NA
NR	NS	NA	19875614	A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose.	Glycemic control in type 1 diabetes (HbA1c)	NA	NA	NA	NA
rs210135	4E-10	NA	19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Hematological parameters	NA	NA	NA	NA
NR	NS	NA	19740415	Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis.	Amyotrophic lateral sclerosis (interaction)	NA	NA	NA	NA
rs2279590, rs11136000, rs9331888	6E-10	NA	19734903	Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease.	Alzheimer's disease	NA	NA	NA	NA
rs6656401, rs3818361	3E-10	NA	19734903	Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease.	Alzheimer's disease	NA	NA	NA	NA
NR	NS	NA	19736353	A genomewide association study points to multiple loci that predict antidepressant drug treatment outcome in depression.	Response to antidepressant treatment	NA	NA	NA	NA
NR	NS	NA	19723657	Colorectal cancer risk is not associated with increased levels of homozygosity in a population from the United Kingdom.	Colorectal cancer	NA	NA	NA	NA
NR	NS	NA	19724244	Genome-wide association study of suicidal ideation emerging during citalopram treatment of depressed outpatients.	Response to antidepressant treatment	NA	NA	NA	NA
NR	NS	NA	19667218	Genome-wide scan of 500,000 single-nucleotide polymorphisms among responders and nonresponders to interferon beta therapy in multiple sclerosis.	Response to interferon beta therapy	NA	NA	NA	NA
NR	NS	NA	19584900	Association of FTO variants with BMI and fat mass in the self-contained population of Sorbs in Germany.	Body mass index and fat mass	NA	NA	NA	NA
NR	NS	NA	19525478	Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study.	Homocysteine levels	NA	NA	NA	NA
NR	NS	NA	19508998	Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene.	Premature ovarian failure	NA	NA	NA	NA
NR	NS	NA	19508968	A genome-wide association study suggests that a locus within the ataxin 2 binding protein 1 gene is associated with hand osteoarthritis: the Treat-OA consortium.	Osteoarthritis	NA	NA	NA	NA
NR	NS	NA	19497516	Identification of a genetic variant associated with abdominal aortic aneurysms on chromosome 3p12.3 by genome wide association.	Abdominal aortic aneurysm	NA	NA	NA	NA
rs2395148, rs3135363, rs2856683, rs9357152	1E-10	NA	19458352	Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.	Primary biliary cirrhosis	NA	NA	NA	NA
rs2395148, rs3135363, rs2856683, rs9357152	7E-10	NA	19458352	Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.	Primary biliary cirrhosis	NA	NA	NA	NA
NR	NS	NA	19448189	A genomewide association study of response to lithium for prevention of recurrence in bipolar disorder.	Response to lithium treatment in bipolar disorder	NA	NA	NA	NA
NR	NS	NA	19442274	Identification of novel genetic susceptibility loci for Behçet's disease using a genome-wide association study.	Behcet's disease	NA	NA	NA	NA
NR	NS	NA	20031582	Comprehensive whole-genome and candidate gene analysis for response to statin therapy in the Treating to New Targets (TNT) cohort.	Response to statin therapy	NA	NA	NA	NA
NR	NS	NA	19282985	Genome-wide association analyses identify SPOCK as a key novel gene underlying age at menarche.	Menarche (age at onset)	NA	NA	NA	NA
NR	NS	NA	19268276	Genome-wide association study of smoking initiation and current smoking.	Smoking behavior	NA	NA	NA	NA
NR	NS	NA	19252134	Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes.	Type 2 diabetes nephropathy	NA	NA	NA	NA
NR	NS	NA	19242412	Identification of IFRD1 as a modifier gene for cystic fibrosis lung disease.	Cystic fibrosis severity	NA	NA	NA	NA
rs2048327,rs3127599,rs7767084,rs10755578	1E-9	NA	19198611	Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.	Coronary heart disease	NA	NA	NA	NA
rs2048327,rs3127599,rs7767084,rs10755578	4E-15	NA	19198611	Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.	Coronary heart disease	NA	NA	NA	NA
NR	NS	NA	19197363	A genome-wide investigation of SNPs and CNVs in schizophrenia.	Schizophrenia	NA	NA	NA	NA
NR	NS	NA	19193627	A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	NA	NA	NA	NA
NR	NS	NA	19188921	Genome-wide association analyses suggested a novel mechanism for smoking behavior regulated by IL15.	Smoking behavior	NA	NA	NA	NA
NR	NS	NA	19181680	Common variants in the region around Osterix are associated with bone mineral density and growth in childhood.	Bone mineral density	NA	NA	NA	NA
NR	NS	NA	19148276	Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI Study.	Polyunsaturated fatty acid levels	NA	NA	NA	NA
Pending	Pending	NA	19114987	Singleton deletions throughout the genome increase risk of bipolar disorder.	Bipolar disorder	NA	NA	NA	NA
NR	NS	NA	19065144	Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo.	Major depressive disorder	NA	NA	NA	NA
NR	NS	NA	19047183	GRM7 variants confer susceptibility to age-related hearing impairment.	Hearing impairment	NA	NA	NA	NA
NR	NS	NA	19009022	Genome-wide association for nicotine dependence and smoking cessation success in NIH research volunteers.	Nicotine dependence	NA	NA	NA	NA
NR	NS	NA	18980221	Genome-wide association scan of attention deficit hyperactivity disorder.	Attention deficit hyperactivity disorder	NA	NA	NA	NA
NR	NS	NA	19802338	Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replication.	Lipid traits	NA	NA	NA	NA
NR	NS	NA	18760390	Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait.	Hearing impairment	NA	NA	NA	NA
NR	NS	NA	18729187	A polygenic model with common variants may predict lung adenocarcinoma risk in humans.	Lung adenocarcinoma	NA	NA	NA	NA
Pending	Pending	NA	18685109	Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome.	TP53 carriage	NA	NA	NA	NA
NR	NS	NA	19165924	Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis.	Sarcoidosis	NA	NA	NA	NA
NR	NS	NA	18519826	Molecular genetics of successful smoking cessation: convergent genome-wide association study results.	Smoking cessation	NA	NA	NA	NA
rs1015362, rs4911414	6E-37	NA	18488028	Two newly identified genetic determinants of pigmentation in Europeans.	Burning and freckling	NA	NA	NA	NA
rs1015362, rs4911414	8E-29	NA	18488028	Two newly identified genetic determinants of pigmentation in Europeans.	Freckles	NA	NA	NA	NA
rs1015362, rs4911414	3E-9	NA	18488028	Two newly identified genetic determinants of pigmentation in Europeans.	Red vs. non-red hair color	NA	NA	NA	NA
rs1015362, rs4911414	2E-24	NA	18488028	Two newly identified genetic determinants of pigmentation in Europeans.	Skin sensitivity to sun	NA	NA	NA	NA
NR	NS	NA	18449908	Genome screen of late-onset Alzheimer's extended pedigrees identifies TRPC4AP by haplotype analysis.	Alzheimer's disease	NA	NA	NA	NA
NR	NS	NA	18360741	The nature of nurture: a genomewide association scan for family chaos.	Environmental confusion in the home	NA	NA	NA	NA
NR	NS	NA	18325910	Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.	Obesity	NA	NA	NA	NA
NR	NS	NA	18317468	Whole-genome association study of bipolar disorder.	Bipolar disorder	NA	NA	NA	NA
NR	NS	NA	18227835	Alpha-5/alpha-3 nicotinic receptor subunit alleles increase risk for heavy smoking.	Nicotine dependence	NA	NA	NA	NA
NR	NS	NA	18067574	Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays.	General cognitive ability	NA	NA	NA	NA
NR	NS	NA	18195134	Genome-wide pharmacogenomic analysis of the response to interferon beta therapy in multiple sclerosis.	Response to interferon beta therapy	NA	NA	NA	NA
NR	NS	NA	18073375	Two genome-wide association studies of aggressive prostate cancer implicate putative prostate tumor suppressor gene DAB2IP.	Prostate cancer	NA	NA	NA	NA
NR	NS	NA	17911428	A genome-wide study of lupus: preliminary analysis and data release.	Lupus	NA	NA	NA	NA
NR	NS	NA	17903299	A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.	Lipid traits	NA	NA	NA	NA
NR	NS	NA	17848626	A 100K genome-wide association scan for diabetes and related traits in the Framingham Heart Study: replication and integration with other genome-wide datasets.	Type 2 diabetes and 6 quantitative traits	NA	NA	NA	NA
NR	NS	NA	17846126	Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations.	Type 2 diabetes	NA	NA	NA	NA
rs11209003,rs11209002,rs2064689,rs1004819,rs2902440,rs11465802,rs2201841,rs11465804,rs11209026,rs1343151,rs10889676,rs10889677,rs9988642,rs12567232,rs6669582,rs10789230	1E-8	NA	17804789	Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.	Crohn's disease	NA	NA	NA	NA
rs11209003,rs11209002,rs2064689,rs1004819,rs2902440,rs11465802,rs2201841,rs11465804,rs11209026,rs1343151,rs10889676,rs10889677,rs9988642,rs12567232,rs6669582,rs10789230	2E-7	NA	17804789	Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.	Crohn's disease	NA	NA	NA	NA
NR	2E-38	NA	17767159	A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.	F-cell distribution	NA	NA	NA	NA
NR	NS	NA	17671248	Whole-genome analysis of sporadic amyotrophic lateral sclerosis.	Amyotrophic lateral sclerosis	NA	NA	NA	NA
NR	9E-6	NA	17505501	Genome-wide pharmacogenetic investigation of a hepatic adverse event without clinical signs of immunopathology suggests an underlying immune pathogenesis.	Response to ximelagatran treatment	NA	NA	NA	NA
NR	NS	NA	17478681	A common allele on chromosome 9 associated with coronary heart disease.	Coronary heart disease	NA	NA	NA	NA
NR	NS	NA	17470457	Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance.	Episodic memory	NA	NA	NA	NA
NR	NS	NA	17407593	Molecular genetics of nicotine dependence and abstinence: whole genome association using 520,000 SNPs.	Nicotine dependence	NA	NA	NA	NA
NR	3E-15	NA	17401366	Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.	Prostate cancer	NA	NA	NA	NA
NR	NS	NA	17357082	Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.	Progressive supranuclear palsy	NA	NA	NA	NA
NR	NS	NA	17223258	Genome-wide single nucleotide polymorphism analysis of lung cancer risk detects the KLF6 gene.	Lung cancer	NA	NA	NA	NA
NR	NS	NA	17053149	Common Kibra alleles are associated with human memory performance.	Memory performance	NA	NA	NA	NA
NR	NS	NA	16614226	A common genetic variant is associated with adult and childhood obesity.	Obesity	NA	NA	NA	NA