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rs12466022

From SNPedia

Orientationplus
Stabilizedplus
Make rs12466022(A;A)
Make rs12466022(A;C)
Make rs12466022(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position43131922
is asnp
is mentioned by
dbSNPrs12466022
ebirs12466022
HLIrs12466022
Exacrs12466022
Varsomers12466022
Maprs12466022
PheGenIrs12466022
hapmaprs12466022
1000 genomesrs12466022
hgdprs12466022
ensemblrs12466022
gopubmedrs12466022
geneviewrs12466022
scholarrs12466022
googlers12466022
pharmgkbrs12466022
gwascentralrs12466022
openSNPrs12466022
23andMers12466022
23andMe allrs12466022
SNP Nexus

SNPshotrs12466022
SNPdbers12466022
MSV3drs12466022
GWAS Ctlgrs12466022
GMAF0.3044
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele C
P-val 6E-10
Odds Ratio 1.1100 1.10-1.13]