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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
dbSNP (classic)rs766903
ClinGenrs766903
ebirs766903
HLIrs766903
Exacrs766903
Gnomadrs766903
Varsomers766903
LitVarrs766903
Maprs766903
PheGenIrs766903
Biobankrs766903
1000 genomesrs766903
hgdprs766903
ensemblrs766903
geneviewrs766903
scholarrs766903
googlers766903
pharmgkbrs766903
gwascentralrs766903
openSNPrs766903
23andMers766903
SNPshotrs766903
SNPdbers766903
MSV3drs766903
GWAS Ctlgrs766903
GMAF0.1754
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 A
P-val 0.000002
Odds Ratio 0.0900 [0.05-0.13] unit decrease