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rs13333054

From SNPedia

Orientationplus
Stabilizedplus
Make rs13333054(C;C)
Make rs13333054(C;T)
Make rs13333054(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position85977427
is asnp
is mentioned by
dbSNPrs13333054
ebirs13333054
HLIrs13333054
Exacrs13333054
Varsomers13333054
Maprs13333054
PheGenIrs13333054
hapmaprs13333054
1000 genomesrs13333054
hgdprs13333054
ensemblrs13333054
gopubmedrs13333054
geneviewrs13333054
scholarrs13333054
googlers13333054
pharmgkbrs13333054
gwascentralrs13333054
openSNPrs13333054
23andMers13333054
23andMe allrs13333054
SNP Nexus

SNPshotrs13333054
SNPdbers13333054
MSV3drs13333054
GWAS Ctlgrs13333054
GMAF0.3017
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait Multiple sclerosis
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele A
P-val 1E-8
Odds Ratio 1.11 [1.1-1.13]