rs9616906
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9616906(A;A) |
Make rs9616906(A;G) |
Make rs9616906(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 50666252 |
is a | snp |
is | mentioned by |
dbSNP | rs9616906 |
dbSNP (classic) | rs9616906 |
ClinGen | rs9616906 |
ebi | rs9616906 |
HLI | rs9616906 |
Exac | rs9616906 |
Gnomad | rs9616906 |
Varsome | rs9616906 |
LitVar | rs9616906 |
Map | rs9616906 |
PheGenI | rs9616906 |
Biobank | rs9616906 |
1000 genomes | rs9616906 |
hgdp | rs9616906 |
ensembl | rs9616906 |
geneview | rs9616906 |
scholar | rs9616906 |
rs9616906 | |
pharmgkb | rs9616906 |
gwascentral | rs9616906 |
openSNP | rs9616906 |
23andMe | rs9616906 |
SNPshot | rs9616906 |
SNPdbe | rs9616906 |
MSV3d | rs9616906 |
GWAS Ctlg | rs9616906 |
GMAF | 0.2902 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20834067![]() |
Trait | |
Title | Joint influence of small-effect genetic variants on human longevity. |
Risk Allele | |
P-val | 0.000001 |
Odds Ratio | None None |