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: 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: 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
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: 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: 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: 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: 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: 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: 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: 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: 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: 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