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.
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
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1 2013 2013
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
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2012 2012
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
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 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
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2018 2018
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2010 2010
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
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
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
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1 2009 2009
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1 2009 2009
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1 2009 2009
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
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
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2019 2019
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1 2009 2009
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
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 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
Idiopathic Pulmonary Fibrosis
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
63 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2011 2011
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
130 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2018 2018
Immune System Diseases
CUI: C0021053
Disease: Immune System Diseases
116 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.800 1.000 1 2011 2011