Have questions? Visit https://www.reddit.com/r/SNPedia

rs10496262

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0
Make rs10496262(G;T)
Make rs10496262(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position81524000
is asnp
is mentioned by
dbSNPrs10496262
ebirs10496262
HLIrs10496262
Exacrs10496262
Varsomers10496262
Maprs10496262
PheGenIrs10496262
hapmaprs10496262
1000 genomesrs10496262
hgdprs10496262
ensemblrs10496262
gopubmedrs10496262
geneviewrs10496262
scholarrs10496262
googlers10496262
pharmgkbrs10496262
gwascentralrs10496262
openSNPrs10496262
23andMers10496262
23andMe allrs10496262
SNP Nexus

SNPshotrs10496262
SNPdbers10496262
MSV3drs10496262
GWAS Ctlgrs10496262
GMAF0.07759
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 17903295OA-icon.png]
Trait Aging traits
Title Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study
Risk Allele
P-val 2.9999999999999999E-7
Odds Ratio NR NR


GET Evidence
rs10496262
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.078125
summary