Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1128334
rs1128334
ETS1
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		A 0.810 GeneticVariation GWASCAT By a genome-wide association study (320 patients and 1,500 controls) and subsequent replication altogether involving a total of 3,300 Asian SLE patients from Hong Kong, Mainland China, and Thailand, as well as 4,200 ethnically and geographically matched controls, genetic variants in ETS1 and WDFY4 were found to be associated with SLE (ETS1: rs1128334, P = 2.33x10(-11), OR = 1.29; WDFY4: rs7097397, P = 8.15x10(-12), OR = 1.30). 20169177

2010
dbSNP: rs1128334
rs1128334
ETS1
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.810 GeneticVariation GWASCAT Identification of a Systemic Lupus Erythematosus Risk Locus Spanning ATG16L2, FCHSD2, and P2RY2 in Koreans. 26663301

2016
dbSNP: rs3802826
rs3802826
ETS1
CUI: C0033860
Disease: Psoriasis
Psoriasis 		A 0.800 GeneticVariation GWASCAT Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 23143594

2012
dbSNP: rs11221332
rs11221332
ETS1
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		A 0.800 GeneticVariation GWASCAT Multiple common variants for celiac disease influencing immune gene expression. 20190752

2010
dbSNP: rs8705
rs8705
ETS1
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs8705
rs8705
ETS1
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs8705
rs8705
ETS1
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs8705
rs8705
ETS1
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs8705
rs8705
ETS1
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs8705
rs8705
ETS1
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs7924522
rs7924522
ETS1
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 GeneticVariation GWASCAT Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma. 30054594

2018
dbSNP: rs7924522
rs7924522
ETS1
CUI: C0017601
Disease: Glaucoma
Glaucoma 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma. 30054594

2018
dbSNP: rs7924522
rs7924522
ETS1
CUI: C0040420
Disease: Tonometry
Tonometry 		C 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998

2018
dbSNP: rs7924522
rs7924522
ETS1
CUI: C0040420
Disease: Tonometry
Tonometry 		C 0.700 GeneticVariation GWASCAT Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma. 29785010

2018
dbSNP: rs7108992
rs7108992
ETS1
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs6590334
rs6590334
ETS1
CUI: C0033860
Disease: Psoriasis
Psoriasis 		T 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility. 25903422

2015
dbSNP: rs4937334
rs4937334
ETS1
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs4937333
rs4937333
ETS1
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs4128561
rs4128561
ETS1
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 GeneticVariation GWASCAT Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci. 25920553

2016
dbSNP: rs3809006
rs3809006
ETS1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.700 GeneticVariation GWASCAT Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. 24076602

2013
dbSNP: rs3802826
rs3802826
ETS1
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		A 0.700 GeneticVariation GWASCAT Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. 26626624

2015
dbSNP: rs34834119
rs34834119
ETS1
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs34834119
rs34834119
ETS1
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs11819995
rs11819995
ETS1
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		T 0.700 GeneticVariation GWASCAT Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population. 30718926

2019
dbSNP: rs116502295
rs116502295
ETS1
CUI: C0869220
Disease: Adverse effects, not elsewhere classified
Adverse effects, not elsewhere classified 		C 0.700 GeneticVariation GWASCAT Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records. 30420678

2019