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rs4764043

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs4764043(C;T)
Make rs4764043(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position13962548
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs4764043
ebirs4764043
HLIrs4764043
Exacrs4764043
Varsomers4764043
Maprs4764043
PheGenIrs4764043
hapmaprs4764043
1000 genomesrs4764043
hgdprs4764043
ensemblrs4764043
gopubmedrs4764043
geneviewrs4764043
scholarrs4764043
googlers4764043
pharmgkbrs4764043
gwascentralrs4764043
openSNPrs4764043
23andMers4764043
23andMe allrs4764043
SNP Nexus

SNPshotrs4764043
SNPdbers4764043
MSV3drs4764043
GWAS Ctlgrs4764043
GMAF0.0404
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21782286OA-icon.png]
Trait
Title A genome-wide association study of aging.
Risk Allele T
P-val 0.000006
Odds Ratio 1.1700 [NR]