rs10168266, STAT4

N. diseases: 8
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.
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
47 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.800 1.000 1 2013 2013
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.710 1.000 2 2014 2017
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.700 1.000 2 2012 2012
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.700 1.000 1 2013 2013
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.010 1.000 1 2016 2016
Neuromyelitis Optica
CUI: C0027873
Disease: Neuromyelitis Optica
45 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.010 1.000 1 2017 2017
Pulmonary Fibrosis
CUI: C0034069
Disease: Pulmonary Fibrosis
25 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.010 1.000 1 2013 2013
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.010 1.000 1 2013 2013