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: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.700 1.000 2 2018 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: 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: rs10174238
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2019 2019
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: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2019 2019
dbSNP: rs10174238
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70
CUI: C1858558
Disease: Rheumatoid Arthritis, Systemic Juvenile
Rheumatoid Arthritis, Systemic Juvenile 		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: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
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: 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: C0027121
Disease: Myositis
Myositis 		0.700 1.000 1 2019 2019
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: rs11684030
rs11684030
STAT4
1.000 0.040 2 191152153 upstream gene variant G/A snv 0.52
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer 		0.700 1.000 1 2019 2019
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: rs11893432
rs11893432
STAT4
0.827 0.120 2 191057148 intron variant C/G snv 0.21
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2012 2012
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
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: rs13389408
rs13389408
STAT4
0.851 0.160 2 191068557 3 prime UTR variant T/C snv 7.4E-02
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2019 2019
dbSNP: rs13389408
rs13389408
STAT4
0.851 0.160 2 191068557 3 prime UTR variant T/C snv 7.4E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2019 2019
dbSNP: rs13389408
rs13389408
STAT4
0.851 0.160 2 191068557 3 prime UTR variant T/C snv 7.4E-02
CUI: C0027121
Disease: Myositis
Myositis 		0.700 1.000 1 2019 2019
dbSNP: rs13389408
rs13389408
STAT4
0.851 0.160 2 191068557 3 prime UTR variant T/C snv 7.4E-02
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.700 1.000 1 2019 2019
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: 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: 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