rs10181656, STAT4

N. diseases: 9
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.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.820 1.000 3 2012 2017
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
89 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.020 1.000 2 2012 2017
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.020 1.000 2 2008 2010
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.010 1.000 1 2014 2014
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.010 1.000 1 2008 2008
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.010 1 2018 2018
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.010 1.000 1 2014 2014
Neuromyelitis Optica
CUI: C0027873
Disease: Neuromyelitis Optica
45 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.010 1.000 1 2017 2017
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.010 1.000 1 2014 2014