rs6489785
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6489785(C;C) |
Make rs6489785(C;T) |
Make rs6489785(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 120925921 |
is a | snp |
is | mentioned by |
dbSNP | rs6489785 |
dbSNP (classic) | rs6489785 |
ClinGen | rs6489785 |
ebi | rs6489785 |
HLI | rs6489785 |
Exac | rs6489785 |
Gnomad | rs6489785 |
Varsome | rs6489785 |
LitVar | rs6489785 |
Map | rs6489785 |
PheGenI | rs6489785 |
Biobank | rs6489785 |
1000 genomes | rs6489785 |
hgdp | rs6489785 |
ensembl | rs6489785 |
geneview | rs6489785 |
scholar | rs6489785 |
rs6489785 | |
pharmgkb | rs6489785 |
gwascentral | rs6489785 |
openSNP | rs6489785 |
23andMe | rs6489785 |
SNPshot | rs6489785 |
SNPdbe | rs6489785 |
MSV3d | rs6489785 |
GWAS Ctlg | rs6489785 |
GMAF | 0.2603 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 |