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.
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 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
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
Uveomeningoencephalitic Syndrome
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
27 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2010 2010
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
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
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
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
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
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 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
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
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
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
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
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
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: 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
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
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