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rs12377462

From SNPedia

Orientationplus
Stabilizedplus
Make rs12377462(C;C)
Make rs12377462(C;T)
Make rs12377462(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position32914591
is asnp
is mentioned by
dbSNPrs12377462
ebirs12377462
HLIrs12377462
Exacrs12377462
Varsomers12377462
Maprs12377462
PheGenIrs12377462
hapmaprs12377462
1000 genomesrs12377462
hgdprs12377462
ensemblrs12377462
gopubmedrs12377462
geneviewrs12377462
scholarrs12377462
googlers12377462
pharmgkbrs12377462
gwascentralrs12377462
openSNPrs12377462
23andMers12377462
23andMe allrs12377462
SNP Nexus

SNPshotrs12377462
SNPdbers12377462
MSV3drs12377462
GWAS Ctlgrs12377462
GMAF0.4022
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22367966]
Trait
Title Genome-wide association study identifies novel loci associated with serum level of vitamin B12 in Chinese men.
Risk Allele
P-val 0.000002
Odds Ratio 28.5300 None