Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7574865
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.900 0.967 7 2007 2017
dbSNP: rs7574865
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.900 1.000 1 2008 2017
dbSNP: rs7574865
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.900 0.966 1 2007 2017
dbSNP: rs7574865
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.900 0.909 1 2013 2019
dbSNP: rs7574865
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.870 0.778 2 2009 2017
dbSNP: rs10181656
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.820 1.000 1 2012 2017
dbSNP: rs7574070
rs7574070
STAT4
1.000 0.200 2 191145762 intron variant A/C snv 0.55
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.810 1.000 2 2012 2015
dbSNP: rs7574865
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.810 1.000 2 2012 2014
dbSNP: rs3821236
rs3821236
STAT4
0.882 0.160 2 191038032 intron variant G/A snv 0.25
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.810 1.000 1 2008 2016
dbSNP: rs7601754
rs7601754
STAT4
0.882 0.160 2 191075725 intron variant G/A;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.810 1.000 1 2010 2013
dbSNP: rs3821236
rs3821236
STAT4
0.882 0.160 2 191038032 intron variant G/A snv 0.25
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.800 1.000 3 2010 2019
dbSNP: rs11889341
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 2 2014 2019
dbSNP: rs13426947
rs13426947
STAT4
0.925 0.200 2 191068528 3 prime UTR variant G/A snv 0.20
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 2 2012 2015
dbSNP: rs1517352
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 2 2012 2015
dbSNP: rs10168266
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome 		0.800 1.000 1 2013 2013
dbSNP: rs10174238
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70
CUI: C3898105
Disease: Oligoarticular Juvenile Idiopathic Arthritis
Oligoarticular Juvenile Idiopathic Arthritis 		0.800 1.000 1 2013 2013
dbSNP: rs3024921
rs3024921
STAT4
0.925 0.120 2 191078546 intron variant A/T snv 3.6E-02
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.800 1.000 1 2012 2012
dbSNP: rs6715106
rs6715106
STAT4
1.000 0.080 2 191048308 intron variant A/G snv 6.1E-02
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 1 2011 2012
dbSNP: rs7572482
rs7572482
STAT4
1.000 0.200 2 191150346 intron variant A/C;G snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 1.000 1 2012 2012
dbSNP: rs7574865
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		0.800 1.000 1 2011 2011
dbSNP: rs7601754
rs7601754
STAT4
0.882 0.160 2 191075725 intron variant G/A;T snv
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.800 1.000 1 2013 2013
dbSNP: rs897200
rs897200
STAT4
0.851 0.280 2 191153045 upstream gene variant T/C snv 0.54
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 1.000 1 2012 2012
dbSNP: rs7582694
rs7582694
STAT4
0.763 0.400 2 191105394 intron variant C/G snv 0.77
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.740 1.000 2 2008 2017
dbSNP: rs11889341
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.710 1.000 4 2015 2018
dbSNP: rs10168266
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.710 1.000 1 2014 2017