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.
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.900 1.000 11 2008 2017
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
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
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.040 1.000 4 2008 2015
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
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
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
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
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
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
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.020 1.000 2 2009 2010
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
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
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
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
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