rs7574865, STAT4

N. diseases: 11
Source: CURATED ×
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
628 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.900 0.967 8 2007 2017
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
1789 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.900 0.966 3 2007 2017
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
231 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.900 1.000 1 2008 2017
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
203 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.900 0.909 1 2013 2019
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
141 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.870 0.778 2 2009 2017
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
609 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.810 1.000 2 2012 2014
Immune System Diseases
CUI: C0021053
Disease: Immune System Diseases
106 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.800 1.000 1 2011 2011
Biliary cirrhosis
CUI: C0023892
Disease: Biliary cirrhosis
36 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.700 1.000 1 2012 2012
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
637 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.700 1.000 1 2011 2011
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
29 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.700 1.000 1 2017 2017
SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 11
CUI: C2677096
Disease: SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 11
1 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.700 0