rs7574865, STAT4

N. diseases: 59
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.
Crohn's disease of large bowel
CUI: C0156147
Disease: Crohn's disease of large bowel
1 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2010 2010
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
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
CUI: C2717865
Disease: Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
3 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2013 2013
Alveolitis, Fibrosing
CUI: C4721507
Disease: Alveolitis, Fibrosing
4 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2011 2011
Hepatitis B Virus-Related Hepatocellular Carcinoma
CUI: C1333977
Disease: Hepatitis B Virus-Related Hepatocellular Carcinoma
8 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.020 1.000 2 2013 2016
Hamman-Rich syndrome
CUI: C0085786
Disease: Hamman-Rich syndrome
8 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2011 2011
Juvenile rheumatoid arthritis
CUI: C3714757
Disease: Juvenile rheumatoid arthritis
10 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.020 0.500 2 2013 2015
Autoimmune thyroid disease
CUI: C0178468
Disease: Autoimmune thyroid disease
15 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2018 2018
Hematological Disease
CUI: C0018939
Disease: Hematological Disease
16 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2009 2009
Polyendocrinopathies, Autoimmune
CUI: C0085409
Disease: Polyendocrinopathies, Autoimmune
21 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.020 0.500 2 2009 2012
Autoimmune hepatitis
CUI: C4721555
Disease: Autoimmune hepatitis
22 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2017 2017
Autoimmune Chronic Hepatitis
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
23 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2017 2017
Pulmonary Fibrosis
CUI: C0034069
Disease: Pulmonary Fibrosis
25 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.020 1.000 2 2013 2017
Uveomeningoencephalitic Syndrome
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
27 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2010 2010
Drug-Induced Liver Disease
CUI: C0860207
Disease: Drug-Induced Liver Disease
29 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2012 2012
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
30 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.020 1.000 2 2012 2018
Adult type dermatomyositis
CUI: C0221056
Disease: Adult type dermatomyositis
31 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2014 2014
Dermatomyositis
CUI: C0011633
Disease: Dermatomyositis
34 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2014 2014
Encephalitis, St. Louis
CUI: C0014060
Disease: Encephalitis, St. Louis
34 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2013 2013
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
Primary Sjögren's syndrome
CUI: C0151449
Disease: Primary Sjögren's syndrome
42 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.030 0.667 3 2010 2013
Lupus Erythematosus
CUI: C0409974
Disease: Lupus Erythematosus
44 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2007 2007
Lupus Vulgaris
CUI: C0024131
Disease: Lupus Vulgaris
44 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2007 2007
Neuromyelitis Optica
CUI: C0027873
Disease: Neuromyelitis Optica
45 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2017 2017
Lupus Erythematosus, Discoid
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
46 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.020 1.000 2 2007 2017