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rs9616906

From SNPedia

Orientationplus
Stabilizedplus
Make rs9616906(A;A)
Make rs9616906(A;G)
Make rs9616906(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position50666252
is asnp
is mentioned by
dbSNPrs9616906
ebirs9616906
HLIrs9616906
Exacrs9616906
Varsomers9616906
Maprs9616906
PheGenIrs9616906
hapmaprs9616906
1000 genomesrs9616906
hgdprs9616906
ensemblrs9616906
gopubmedrs9616906
geneviewrs9616906
scholarrs9616906
googlers9616906
pharmgkbrs9616906
gwascentralrs9616906
openSNPrs9616906
23andMers9616906
23andMe allrs9616906
SNP Nexus

SNPshotrs9616906
SNPdbers9616906
MSV3drs9616906
GWAS Ctlgrs9616906
GMAF0.2902
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20834067OA-icon.png]
Trait
Title Joint influence of small-effect genetic variants on human longevity.
Risk Allele
P-val 0.000001
Odds Ratio None None