Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2111485
rs2111485 		0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 2 2012 2016
dbSNP: rs2111485
rs2111485 		0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 1 2012 2012
dbSNP: rs2111485
rs2111485 		0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.710 1.000 1 2011 2015
dbSNP: rs2111485
rs2111485 		0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 3 2012 2016
dbSNP: rs2111485
rs2111485 		0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 2 2015 2017
dbSNP: rs2111485
rs2111485 		0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 2 2015 2016
dbSNP: rs2111485
rs2111485 		0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2111485
rs2111485 		0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs2111485
rs2111485 		0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs2111485
rs2111485 		0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2019 2019
dbSNP: rs2111485
rs2111485 		0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2111485
rs2111485 		0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016