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: rs7568275
rs7568275
STAT4
0.827 0.120 2 191101726 intron variant G/C;T snv
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs7568275
rs7568275
STAT4
0.827 0.120 2 191101726 intron variant G/C;T snv
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019
dbSNP: rs7568275
rs7568275
STAT4
0.827 0.120 2 191101726 intron variant G/C;T snv
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs7568275
rs7568275
STAT4
0.827 0.120 2 191101726 intron variant G/C;T snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2019 2019
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: 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: 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: 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: rs7574865
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C0023892
Disease: Biliary cirrhosis
Biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs13401064
rs13401064
STAT4
1.000 0.080 2 191105604 intron variant C/G snv 8.5E-02
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2016 2016
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: rs6749371
rs6749371
STAT4
0.925 0.200 2 191037458 intron variant A/T snv 7.3E-02
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2016 2016
dbSNP: rs6752770
rs6752770
STAT4
1.000 0.080 2 191108837 intron variant A/G snv 0.31
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2011 2011
dbSNP: rs1517352
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2015 2015
dbSNP: rs10174238
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs7582694
rs7582694
STAT4
0.763 0.400 2 191105394 intron variant C/G snv 0.77
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2019 2019
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: 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: rs13390936
rs13390936
STAT4
0.925 0.080 2 191090090 intron variant A/T snv 8.4E-02
CUI: C4706572
Disease: Invasive non-typhoidal salmonellosis
Invasive non-typhoidal salmonellosis 		0.700 1.000 1 2018 2018
dbSNP: rs10174238
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70
CUI: C2931171
Disease: Juvenile pauciarticular chronic arthritis
Juvenile pauciarticular chronic arthritis 		0.700 1.000 1 2013 2013
dbSNP: rs10174238
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70
CUI: C0087031
Disease: Juvenile-Onset Still Disease
Juvenile-Onset Still Disease 		0.700 1.000 1 2013 2013
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: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.900 0.967 7 2007 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: 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