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.
SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 11
1 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.700 0
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
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
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
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
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
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
Diabetes Mellitus, Insulin-Dependent
954 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.070 0.571 7 2008 2015
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
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.040 0.750 4 2008 2015
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.870 0.778 9 2009 2017
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.050 0.800 5 2010 2015
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
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.900 0.966 29 2007 2017
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.900 0.967 30 2007 2017
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