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rs9568281

From SNPedia

Orientationplus
Stabilizedplus
Make rs9568281(A;A)
Make rs9568281(A;G)
Make rs9568281(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position49611068
is asnp
is mentioned by
dbSNPrs9568281
ebirs9568281
HLIrs9568281
Exacrs9568281
Varsomers9568281
Maprs9568281
PheGenIrs9568281
hapmaprs9568281
1000 genomesrs9568281
hgdprs9568281
ensemblrs9568281
gopubmedrs9568281
geneviewrs9568281
scholarrs9568281
googlers9568281
pharmgkbrs9568281
gwascentralrs9568281
openSNPrs9568281
23andMers9568281
23andMe allrs9568281
SNP Nexus

SNPshotrs9568281
SNPdbers9568281
MSV3drs9568281
GWAS Ctlgrs9568281
GMAF0.1019
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23412934OA-icon.png]
Trait Multiple sclerosis
Title A genome-wide association study of brain lesion distribution in multiple sclerosis.
Risk Allele
P-val 3E-7
Odds Ratio NR NR