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rs766903

From SNPedia

Orientationminus
Stabilizedminus
Make rs766903(C;C)
Make rs766903(C;T)
Make rs766903(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position51310050
GeneBIN2
is asnp
is mentioned by
dbSNPrs766903
ebirs766903
HLIrs766903
Exacrs766903
Varsomers766903
Maprs766903
PheGenIrs766903
hapmaprs766903
1000 genomesrs766903
hgdprs766903
ensemblrs766903
gopubmedrs766903
geneviewrs766903
scholarrs766903
googlers766903
pharmgkbrs766903
gwascentralrs766903
openSNPrs766903
23andMers766903
23andMe allrs766903
SNP Nexus

SNPshotrs766903
SNPdbers766903
MSV3drs766903
GWAS Ctlgrs766903
GMAF0.1754
Max Magnitude
? (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 A
P-val 0.000002
Odds Ratio 0.0900 [0.05-0.13] unit decrease