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rs7315621

From SNPedia

Orientationplus
Stabilizedplus
Make rs7315621(A;A)
Make rs7315621(A;G)
Make rs7315621(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position131600651
is asnp
is mentioned by
dbSNPrs7315621
ebirs7315621
HLIrs7315621
Exacrs7315621
Varsomers7315621
Maprs7315621
PheGenIrs7315621
hapmaprs7315621
1000 genomesrs7315621
hgdprs7315621
ensemblrs7315621
gopubmedrs7315621
geneviewrs7315621
scholarrs7315621
googlers7315621
pharmgkbrs7315621
gwascentralrs7315621
openSNPrs7315621
23andMers7315621
23andMe allrs7315621
SNP Nexus

SNPshotrs7315621
SNPdbers7315621
MSV3drs7315621
GWAS Ctlgrs7315621
GMAF0.404
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