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
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
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, 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
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
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
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
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
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
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
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
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
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
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
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2010 2010
Crohn's disease of large bowel
CUI: C0156147
Disease: Crohn's disease of large bowel
1 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2010 2010
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
Alveolitis, Fibrosing
CUI: C4721507
Disease: Alveolitis, Fibrosing
4 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2011 2011
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