rs766903
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs766903(C;C) |
| Make rs766903(C;T) |
| Make rs766903(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 51310050 |
| Gene | BIN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs766903 |
| dbSNP (classic) | rs766903 |
| ClinGen | rs766903 |
| ebi | rs766903 |
| HLI | rs766903 |
| Exac | rs766903 |
| Gnomad | rs766903 |
| Varsome | rs766903 |
| LitVar | rs766903 |
| Map | rs766903 |
| PheGenI | rs766903 |
| Biobank | rs766903 |
| 1000 genomes | rs766903 |
| hgdp | rs766903 |
| ensembl | rs766903 |
| geneview | rs766903 |
| scholar | rs766903 |
| rs766903 | |
| pharmgkb | rs766903 |
| gwascentral | rs766903 |
| openSNP | rs766903 |
| 23andMe | rs766903 |
| SNPshot | rs766903 |
| SNPdbe | rs766903 |
| MSV3d | rs766903 |
| GWAS Ctlg | rs766903 |
| GMAF | 0.1754 |
| 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 | A |
| P-val | 0.000002 |
| Odds Ratio | 0.0900 [0.05-0.13] unit decrease |
