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: 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: rs10174238
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70
CUI: C1384600
Disease: Systemic onset juvenile chronic arthritis
Systemic onset juvenile 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: C3890205
Disease: Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative 		0.700 1.000 1 2013 2013
dbSNP: rs10553577
rs10553577
STAT4
1.000 0.200 2 191090464 intron variant ATAATA/-;ATA;ATAATAATA delins
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome 		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: 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: rs9967792
rs9967792
STAT4
1.000 0.080 2 191109709 intron variant T/C snv 0.65
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2013 2013
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: rs11893432
rs11893432
STAT4
0.827 0.120 2 191057148 intron variant C/G snv 0.21
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.700 1.000 2 2014 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
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: 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: rs1517352
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2015 2015
dbSNP: rs6736175
rs6736175
STAT4
1.000 0.080 2 191081596 intron variant C/T snv 0.45
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2015 2015
dbSNP: rs12612769
rs12612769
STAT4
1.000 0.080 2 191089272 intron variant A/C;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2016 2016
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: rs199559999
rs199559999
STAT4
1.000 0.040 2 191090480 intron variant TAC/- del
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2016 2016
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: rs6749371
rs6749371
STAT4
0.925 0.200 2 191037458 intron variant A/T snv 7.3E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2016 2016
dbSNP: rs11889341
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome 		0.700 1.000 1 2017 2017
dbSNP: rs7568275
rs7568275
STAT4
0.827 0.120 2 191101726 intron variant G/C;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2017 2017
dbSNP: rs7574865
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome 		0.700 1.000 1 2017 2017
dbSNP: rs10174238
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.700 1.000 2 2018 2019
dbSNP: rs10174238
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70
CUI: C0748540
Disease: Scleroderma, Limited
Scleroderma, Limited 		0.700 1.000 1 2018 2018
dbSNP: rs11893432
rs11893432
STAT4
0.827 0.120 2 191057148 intron variant C/G snv 0.21
CUI: C0748540
Disease: Scleroderma, Limited
Scleroderma, Limited 		0.700 1.000 1 2018 2018