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.
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
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
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 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