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rs13008689

From SNPedia

Orientationplus
Stabilizedplus
Make rs13008689(A;A)
Make rs13008689(A;G)
Make rs13008689(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position8390126
is asnp
is mentioned by
dbSNPrs13008689
dbSNP (classic)rs13008689
ClinGenrs13008689
ebirs13008689
HLIrs13008689
Exacrs13008689
Gnomadrs13008689
Varsomers13008689
LitVarrs13008689
Maprs13008689
PheGenIrs13008689
Biobankrs13008689
1000 genomesrs13008689
hgdprs13008689
ensemblrs13008689
geneviewrs13008689
scholarrs13008689
googlers13008689
pharmgkbrs13008689
gwascentralrs13008689
openSNPrs13008689
23andMers13008689
SNPshotrs13008689
SNPdbers13008689
MSV3drs13008689
GWAS Ctlgrs13008689
GMAF0.3659
Max Magnitude0
? (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