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rs9275563

From SNPedia

Orientationplus
Stabilizedplus
Make rs9275563(C;C)
Make rs9275563(C;T)
Make rs9275563(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32710135
is asnp
is mentioned by
dbSNPrs9275563
ebirs9275563
HLIrs9275563
Exacrs9275563
Varsomers9275563
Maprs9275563
PheGenIrs9275563
hapmaprs9275563
1000 genomesrs9275563
hgdprs9275563
ensemblrs9275563
gopubmedrs9275563
geneviewrs9275563
scholarrs9275563
googlers9275563
pharmgkbrs9275563
gwascentralrs9275563
openSNPrs9275563
23andMers9275563
23andMe allrs9275563
SNP Nexus

SNPshotrs9275563
SNPdbers9275563
MSV3drs9275563
GWAS Ctlgrs9275563
GMAF0.4403
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23472185OA-icon.png]
Trait Multiple sclerosis (OCB status)
Title Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.
Risk Allele
P-val 6E-11
Odds Ratio 1.75 [1.47-2.04]