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.
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
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
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.700 1.000 1 2011 2011
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.810 1.000 3 2012 2014
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
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
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
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
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.900 0.909 11 2013 2019
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.060 1.000 6 2013 2019
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
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.020 1.000 2 2013 2013
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
128 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.020 0.500 2 2013 2015
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
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
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
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
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1 2013 2013
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.020 1.000 2 2014 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
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.050 1.000 5 2015 2020
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.030 1.000 3 2015 2019
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