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rs41281112

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs41281112(C;T)
Make rs41281112(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position99866380
GeneCLYBL, LOC101927437
is asnp
is mentioned by
dbSNPrs41281112
dbSNP (classic)rs41281112
ClinGenrs41281112
ebirs41281112
HLIrs41281112
Exacrs41281112
Gnomadrs41281112
Varsomers41281112
LitVarrs41281112
Maprs41281112
PheGenIrs41281112
Biobankrs41281112
1000 genomesrs41281112
hgdprs41281112
ensemblrs41281112
geneviewrs41281112
scholarrs41281112
googlers41281112
pharmgkbrs41281112
gwascentralrs41281112
openSNPrs41281112
23andMers41281112
SNPshotrs41281112
SNPdbers41281112
MSV3drs41281112
GWAS Ctlgrs41281112
GMAF0.02433
Max Magnitude0
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 9E-10
Odds Ratio 83.6000 None