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rs9271588

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0.57x risk for Sjogren's syndrome
(C;T) 0.57x risk for Sjogren's syndrome
(T;T) normal
ReferenceGRCh38 38.1/142
Chromosome6
Position32623176
is asnp
is mentioned by
dbSNPrs9271588
ebirs9271588
HLIrs9271588
Exacrs9271588
Varsomers9271588
Maprs9271588
PheGenIrs9271588
hapmaprs9271588
1000 genomesrs9271588
hgdprs9271588
ensemblrs9271588
gopubmedrs9271588
geneviewrs9271588
scholarrs9271588
googlers9271588
pharmgkbrs9271588
gwascentralrs9271588
openSNPrs9271588
23andMers9271588
23andMe allrs9271588
SNP Nexus

SNPshotrs9271588
SNPdbers9271588
MSV3drs9271588
GWAS Ctlgrs9271588
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24097066]
Trait Sjögren's syndrome
Title A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23.
Risk Allele T
P-val 9E-37
Odds Ratio 1.75 [1.59-1.89]