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.
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
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
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 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 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
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
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
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
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
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
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
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 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
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
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
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
Myasthenia Gravis
CUI: C0026896
Disease: Myasthenia Gravis
93 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2018 2018
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
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
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