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rs6813479

From SNPedia

Orientationplus
Stabilizedplus
Make rs6813479(A;A)
Make rs6813479(A;T)
Make rs6813479(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position136739228
is asnp
is mentioned by
dbSNPrs6813479
ebirs6813479
HLIrs6813479
Exacrs6813479
Varsomers6813479
Maprs6813479
PheGenIrs6813479
hapmaprs6813479
1000 genomesrs6813479
hgdprs6813479
ensemblrs6813479
gopubmedrs6813479
geneviewrs6813479
scholarrs6813479
googlers6813479
pharmgkbrs6813479
gwascentralrs6813479
openSNPrs6813479
23andMers6813479
23andMe allrs6813479
SNP Nexus

SNPshotrs6813479
SNPdbers6813479
MSV3drs6813479
GWAS Ctlgrs6813479
GMAF0.4596
Max Magnitude
? (A;A) (A;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