Source: ALL
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.
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6
1 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.700 0
Diabetes Mellitus, Insulin-Dependent
954 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 1.000 0.950 80 2004 2020
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.900 0.972 36 2004 2019
Encephalitis, St. Louis
CUI: C0014060
Disease: Encephalitis, St. Louis
34 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.030 1.000 3 2004 2014
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.900 0.980 101 2005 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 1.000 0.877 81 2005 2019
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.900 0.857 14 2005 2019
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.860 0.800 10 2005 2016
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.860 0.900 10 2005 2018
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
128 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.090 0.889 9 2005 2015
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.060 0.833 6 2005 2018
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.050 0.600 5 2005 2016
Juvenile rheumatoid arthritis
CUI: C3714757
Disease: Juvenile rheumatoid arthritis
10 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.050 1.000 5 2005 2015
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.030 0.667 3 2005 2019
Generalized vitiligo
CUI: C1304470
Disease: Generalized vitiligo
16 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.030 1.000 3 2005 2008
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.030 1.000 3 2005 2013
Addison Disease
CUI: C0001403
Disease: Addison Disease
13 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.020 1.000 2 2005 2012
Autoimmune thyroid disease
CUI: C0178468
Disease: Autoimmune thyroid disease
15 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.020 1.000 2 2005 2010
Primary Sjögren's syndrome
CUI: C0151449
Disease: Primary Sjögren's syndrome
42 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.010 1 2005 2005
Seropositive rheumatoid arthritis
CUI: C0409651
Disease: Seropositive rheumatoid arthritis
1 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.010 1.000 1 2005 2005
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.760 0.857 7 2006 2019
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.850 0.667 6 2006 2017
Alopecia Areata
CUI: C0002171
Disease: Alopecia Areata
54 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.740 1.000 5 2006 2019
Alopecia
CUI: C0002170
Disease: Alopecia
375 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.040 1.000 4 2006 2019
Autoimmune thyroiditis
CUI: C0920350
Disease: Autoimmune thyroiditis
76 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.720 1.000 4 2006 2015