Source: GWASCAT ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Immune System Diseases
CUI: C0021053
Disease: Immune System Diseases
17 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.800 1.000 1 2011 2012
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
17 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.850 0.667 1 2006 2017
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
616 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.860 0.800 4 2005 2016
Vitiligo
CUI: C0042900
Disease: Vitiligo
87 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.860 0.900 2 2005 2018
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
439 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.900 0.972 6 2004 2019
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
145 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.900 0.980 2 2005 2019
Graves Disease
CUI: C0018213
Disease: Graves Disease
57 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.900 0.857 1 2005 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
399 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 1.000 0.877 12 2005 2019
Diabetes Mellitus, Insulin-Dependent
198 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 1.000 0.950 6 2004 2020