Source: ALL

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: 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: 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 5 2015 2018
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: rs11889341
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21
CUI: C0024131
Disease: Lupus Vulgaris
Lupus Vulgaris 		0.010 1.000 1 2018 2018
dbSNP: rs11889341
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
Lupus Erythematosus, Discoid 		0.010 1.000 1 2018 2018
dbSNP: rs11889341
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.010 < 0.001 1 2011 2011
dbSNP: rs11889341
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21
CUI: C0024143
Disease: Lupus Nephritis
Lupus Nephritis 		0.010 1.000 1 2013 2013
dbSNP: rs11889341
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.010 1.000 1 2014 2014
dbSNP: rs11889341
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21
CUI: C0409974
Disease: Lupus Erythematosus
Lupus Erythematosus 		0.010 1.000 1 2018 2018
dbSNP: rs11889341
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.010 1.000 1 2009 2009
dbSNP: rs11889341
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.010 1.000 1 2015 2015
dbSNP: rs11889341
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2010 2010