Disease: Sjogren's Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10168266
rs10168266
Entrez Id: 6775
Gene Symbol: STAT4
STAT4
CUI: C1527336
Disease:
Sjogren's Syndrome 		T 0.800 GeneticVariation GWASDB A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23. 24097066 2013
dbSNP: rs10168266
rs10168266
Entrez Id: 6775
Gene Symbol: STAT4
STAT4
CUI: C1527336
Disease:
Sjogren's Syndrome 		T 0.800 GeneticVariation GWASCAT A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23. 24097066 2013
dbSNP: rs11889341
rs11889341
Entrez Id: 6775
Gene Symbol: STAT4
STAT4
CUI: C1527336
Disease:
Sjogren's Syndrome 		0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899 2017
dbSNP: rs7574865
rs7574865
Entrez Id: 6775
Gene Symbol: STAT4
STAT4
CUI: C1527336
Disease:
Sjogren's Syndrome 		0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899 2017
dbSNP: rs10553577
rs10553577
Entrez Id: 6775
Gene Symbol: STAT4
STAT4
CUI: C1527336
Disease:
Sjogren's Syndrome 		T 0.700 GeneticVariation GWASCAT Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome. 24097067 2013