rs11889341, STAT4

N. diseases: 12
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 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.800 1.000 2 2014 2019
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.710 1.000 5 2015 2018
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
47 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.700 1.000 1 2017 2017
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.010 1 2011 2011
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.010 1.000 1 2015 2015
Lupus Erythematosus
CUI: C0409974
Disease: Lupus Erythematosus
44 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.010 1.000 1 2018 2018
Lupus Erythematosus, Discoid
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
46 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.010 1.000 1 2018 2018
Lupus Nephritis
CUI: C0024143
Disease: Lupus Nephritis
64 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.010 1.000 1 2013 2013
Lupus Vulgaris
CUI: C0024131
Disease: Lupus Vulgaris
44 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.010 1.000 1 2018 2018
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.010 1.000 1 2014 2014
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.010 1.000 1 2009 2009
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.010 1.000 1 2010 2010