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rs3106598

From SNPedia

Orientationplus
Stabilizedplus
Make rs3106598(A;A)
Make rs3106598(A;G)
Make rs3106598(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position61104778
is asnp
is mentioned by
dbSNPrs3106598
ebirs3106598
HLIrs3106598
Exacrs3106598
Varsomers3106598
Maprs3106598
PheGenIrs3106598
hapmaprs3106598
1000 genomesrs3106598
hgdprs3106598
ensemblrs3106598
gopubmedrs3106598
geneviewrs3106598
scholarrs3106598
googlers3106598
pharmgkbrs3106598
gwascentralrs3106598
openSNPrs3106598
23andMers3106598
23andMe allrs3106598
SNP Nexus

SNPshotrs3106598
SNPdbers3106598
MSV3drs3106598
GWAS Ctlgrs3106598
GMAF0.449
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