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rs6489785

From SNPedia

Orientationplus
Stabilizedplus
Make rs6489785(C;C)
Make rs6489785(C;T)
Make rs6489785(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position120925921
is asnp
is mentioned by
dbSNPrs6489785
ebirs6489785
HLIrs6489785
Exacrs6489785
Varsomers6489785
Maprs6489785
PheGenIrs6489785
hapmaprs6489785
1000 genomesrs6489785
hgdprs6489785
ensemblrs6489785
gopubmedrs6489785
geneviewrs6489785
scholarrs6489785
googlers6489785
pharmgkbrs6489785
gwascentralrs6489785
openSNPrs6489785
23andMers6489785
23andMe allrs6489785
SNP Nexus

SNPshotrs6489785
SNPdbers6489785
MSV3drs6489785
GWAS Ctlgrs6489785
GMAF0.2603
Max Magnitude
? (C;C) (C;T) (T;T) 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