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rs16852912

From SNPedia

Orientationplus
Stabilizedplus
Make rs16852912(C;C)
Make rs16852912(C;T)
Make rs16852912(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position168968888
is asnp
is mentioned by
dbSNPrs16852912
ebirs16852912
HLIrs16852912
Exacrs16852912
Varsomers16852912
Maprs16852912
PheGenIrs16852912
hapmaprs16852912
1000 genomesrs16852912
hgdprs16852912
ensemblrs16852912
gopubmedrs16852912
geneviewrs16852912
scholarrs16852912
googlers16852912
pharmgkbrs16852912
gwascentralrs16852912
openSNPrs16852912
23andMers16852912
23andMe allrs16852912
SNP Nexus

SNPshotrs16852912
SNPdbers16852912
MSV3drs16852912
GWAS Ctlgrs16852912
GMAF0.05877
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 0.000003
Odds Ratio 1.1800 [NR]