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rs11162963

From SNPedia

Orientationplus
Stabilizedplus
Make rs11162963(C;C)
Make rs11162963(C;T)
Make rs11162963(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position80268896
is asnp
is mentioned by
dbSNPrs11162963
ebirs11162963
HLIrs11162963
Exacrs11162963
Varsomers11162963
Maprs11162963
PheGenIrs11162963
hapmaprs11162963
1000 genomesrs11162963
hgdprs11162963
ensemblrs11162963
gopubmedrs11162963
geneviewrs11162963
scholarrs11162963
googlers11162963
pharmgkbrs11162963
gwascentralrs11162963
openSNPrs11162963
23andMers11162963
23andMe allrs11162963
SNP Nexus

SNPshotrs11162963
SNPdbers11162963
MSV3drs11162963
GWAS Ctlgrs11162963
GMAF0.4431
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21782286OA-icon.png]
Trait
Title A genome-wide association study of aging.
Risk Allele T
P-val 0.000004
Odds Ratio 1.0900 [NR]