rs10516487, BANK1

N. diseases: 11
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.
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 0.880 1.000 9 2008 2019
Encephalitis, St. Louis
CUI: C0014060
Disease: Encephalitis, St. Louis
34 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 0.020 1.000 2 2011 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 0.020 0.500 2 2009 2017
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 0.020 1.000 2 2009 2010
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 0.010 1.000 1 2017 2017
Diffuse Scleroderma
CUI: C1258104
Disease: Diffuse Scleroderma
5 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 0.010 1.000 1 2009 2009
Graft-vs-Host Disease
CUI: C0018133
Disease: Graft-vs-Host Disease
25 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 0.010 1.000 1 2016 2016
Hemophilia A
CUI: C0019069
Disease: Hemophilia A
295 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 0.010 1.000 1 2019 2019
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 0.700 1.000 1 2011 2011
Primary Sjögren's syndrome
CUI: C0151449
Disease: Primary Sjögren's syndrome
42 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 0.010 1.000 1 2013 2013
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 0.010 1.000 1 2011 2011