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rs7493138

From SNPedia

Orientationplus
Stabilizedplus
Make rs7493138(C;C)
Make rs7493138(C;T)
Make rs7493138(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position28552722
is asnp
is mentioned by
dbSNPrs7493138
ebirs7493138
HLIrs7493138
Exacrs7493138
Varsomers7493138
Maprs7493138
PheGenIrs7493138
hapmaprs7493138
1000 genomesrs7493138
hgdprs7493138
ensemblrs7493138
gopubmedrs7493138
geneviewrs7493138
scholarrs7493138
googlers7493138
pharmgkbrs7493138
gwascentralrs7493138
openSNPrs7493138
23andMers7493138
23andMe allrs7493138
SNP Nexus

SNPshotrs7493138
SNPdbers7493138
MSV3drs7493138
GWAS Ctlgrs7493138
GMAF0.3039
Max Magnitude
? (C;C) (C;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