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.
EXCESS LMW-DNA
CUI: C1835309
Disease: EXCESS LMW-DNA
9 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.700 0
EXCESS LYMPHOCYTE LOW MOLECULAR WEIGHT DNA
9 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.700 0
RHEUMATOID ARTHRITIS, SUSCEPTIBILITY TO
1 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.700 0
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6
1 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.700 0
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
1878 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 1.000 0.877 83 2004 2017
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
674 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.900 0.955 26 2004 2018
Encephalitis, St. Louis
CUI: C0014060
Disease: Encephalitis, St. Louis
11 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.010 1.000 1 2004 2004
Diabetes Mellitus, Insulin-Dependent
775 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 1.000 0.935 69 2005 2017
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
141 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.100 0.981 53 2005 2018
Vitiligo
CUI: C0042900
Disease: Vitiligo
205 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.850 1.000 9 2005 2017
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
956 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.850 0.600 9 2005 2017
Graves Disease
CUI: C0018213
Disease: Graves Disease
213 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.870 1.000 8 2005 2018
Autoimmune thyroid disease
CUI: C0178468
Disease: Autoimmune thyroid disease
79 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.740 1.000 6 2005 2016
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
94 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.060 0.833 6 2006 2016
Early Rheumatoid Arthritis
CUI: C3899278
Disease: Early Rheumatoid Arthritis
4 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.030 1.000 3 2006 2011
Juvenile rheumatoid arthritis
CUI: C3714757
Disease: Juvenile rheumatoid arthritis
4 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.030 1.000 3 2006 2014
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
44 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.810 1.000 2 2006 2013
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
42 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.020 1.000 2 2006 2011
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
39 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.020 0.500 2 2006 2015
Autoimmune Primary Adrenal Insufficiency
16 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.020 1.000 2 2006 2009
Autoimmune thyroiditis
CUI: C0920350
Disease: Autoimmune thyroiditis
6 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.010 1.000 1 2006 2006
Addison Disease
CUI: C0001403
Disease: Addison Disease
8 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.010 1.000 1 2006 2006
Diabetes
CUI: C0011847
Disease: Diabetes
349 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.030 1.000 3 2007 2015
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
149 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.030 0.667 3 2007 2011
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
440 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.030 1.000 3 2007 2015