rs16852912
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16852912(C;C) |
Make rs16852912(C;T) |
Make rs16852912(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 168968888 |
is a | snp |
is | mentioned by |
dbSNP | rs16852912 |
dbSNP (classic) | rs16852912 |
ClinGen | rs16852912 |
ebi | rs16852912 |
HLI | rs16852912 |
Exac | rs16852912 |
Gnomad | rs16852912 |
Varsome | rs16852912 |
LitVar | rs16852912 |
Map | rs16852912 |
PheGenI | rs16852912 |
Biobank | rs16852912 |
1000 genomes | rs16852912 |
hgdp | rs16852912 |
ensembl | rs16852912 |
geneview | rs16852912 |
scholar | rs16852912 |
rs16852912 | |
pharmgkb | rs16852912 |
gwascentral | rs16852912 |
openSNP | rs16852912 |
23andMe | rs16852912 |
SNPshot | rs16852912 |
SNPdbe | rs16852912 |
MSV3d | rs16852912 |
GWAS Ctlg | rs16852912 |
GMAF | 0.05877 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21782286] |
Trait | |
Title | A genome-wide association study of aging. |
Risk Allele | T |
P-val | 0.000003 |
Odds Ratio | 1.1800 [NR] |