rs3733197, BANK1

N. diseases: 13
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 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.040 1.000 4 2009 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.030 1.000 3 2009 2017
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.020 1.000 2 2009 2010
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.010 1.000 1 2017 2017
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.010 1.000 1 2013 2013
Dermatomyositis
CUI: C0011633
Disease: Dermatomyositis
34 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.010 1.000 1 2019 2019
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.010 1.000 1 2019 2019
Diabetes Mellitus, Insulin-Dependent
954 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.010 1.000 1 2014 2014
Diffuse Scleroderma
CUI: C1258104
Disease: Diffuse Scleroderma
5 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.010 1.000 1 2009 2009
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.010 1.000 1 2010 2010
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.010 1.000 1 2013 2013
MYOTONIC DYSTROPHY 1
CUI: C3250443
Disease: MYOTONIC DYSTROPHY 1
14 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.010 1.000 1 2019 2019
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.010 1.000 1 2011 2011