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.
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
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
SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 11
CUI: C2677096
Disease: SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 11
1 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.700 0
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
47 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.700 1.000 1 2017 2017
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
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
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
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
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
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
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
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
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
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
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 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
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
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
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
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
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
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
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
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