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rs9592783

From SNPedia

Orientationplus
Stabilizedplus
Make rs9592783(A;A)
Make rs9592783(A;G)
Make rs9592783(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position71309082
is asnp
is mentioned by
dbSNPrs9592783
ebirs9592783
HLIrs9592783
Exacrs9592783
Varsomers9592783
Maprs9592783
PheGenIrs9592783
hapmaprs9592783
1000 genomesrs9592783
hgdprs9592783
ensemblrs9592783
gopubmedrs9592783
geneviewrs9592783
scholarrs9592783
googlers9592783
pharmgkbrs9592783
gwascentralrs9592783
openSNPrs9592783
23andMers9592783
23andMe allrs9592783
SNP Nexus

SNPshotrs9592783
SNPdbers9592783
MSV3drs9592783
GWAS Ctlgrs9592783
GMAF0.2208
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