rs9271588

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)		0.57x risk for Sjogren's syndrome
(C;T)		0.57x risk for Sjogren's syndrome
(T;T)		normal

Reference

GRCh38 38.1/142

Chromosome

6

Position

32623176

is a	snp
is	mentioned by
dbSNP	rs9271588
dbSNP (classic)	rs9271588
ClinGen	rs9271588
ebi	rs9271588
HLI	rs9271588
Exac	rs9271588
Gnomad	rs9271588
Varsome	rs9271588
LitVar	rs9271588
Map	rs9271588
PheGenI	rs9271588
Biobank	rs9271588
1000 genomes	rs9271588
hgdp	rs9271588
ensembl	rs9271588
geneview	rs9271588
scholar	rs9271588
google	rs9271588
pharmgkb	rs9271588
gwascentral	rs9271588
openSNP	rs9271588
23andMe	rs9271588
SNPshot	rs9271588
SNPdbe	rs9271588
MSV3d	rs9271588
GWAS Ctlg	rs9271588

Max Magnitude

0

?	(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]