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rs1327328

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) normal
(C;T) normal
(T;T) 1.7x increased risk for multiple sclerosis
ReferenceGRCh38 38.1/141
Chromosome13
Position89750579
is asnp
is mentioned by
dbSNPrs1327328
ebirs1327328
HLIrs1327328
Exacrs1327328
Varsomers1327328
Maprs1327328
PheGenIrs1327328
hapmaprs1327328
1000 genomesrs1327328
hgdprs1327328
ensemblrs1327328
gopubmedrs1327328
geneviewrs1327328
scholarrs1327328
googlers1327328
pharmgkbrs1327328
gwascentralrs1327328
openSNPrs1327328
23andMers1327328
23andMe allrs1327328
SNP Nexus

SNPshotrs1327328
SNPdbers1327328
MSV3drs1327328
GWAS Ctlgrs1327328
GMAF0.3802
Max Magnitude
? (C;C) (C;T) (T;T) 28
rs1327328 is a SNP on chromosome 13.

In a study of two cohorts (Spanish and American multiple sclerosis patients, each numbering several hundred), rs1327328 was one of eight SNPs associated with increased risk for multiple sclerosis. The odds ratio was 1.7 (CI: 1.2 - 2.5, p = 0.0042).[PMID 18941528OA-icon.png]