rs2516739
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2516739(C;C) |
| Make rs2516739(C;T) |
| Make rs2516739(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 2047157 |
| Gene | NTHL1, TSC2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2516739 |
| dbSNP (classic) | rs2516739 |
| ClinGen | rs2516739 |
| ebi | rs2516739 |
| HLI | rs2516739 |
| Exac | rs2516739 |
| Gnomad | rs2516739 |
| Varsome | rs2516739 |
| LitVar | rs2516739 |
| Map | rs2516739 |
| PheGenI | rs2516739 |
| Biobank | rs2516739 |
| 1000 genomes | rs2516739 |
| hgdp | rs2516739 |
| ensembl | rs2516739 |
| geneview | rs2516739 |
| scholar | rs2516739 |
| rs2516739 | |
| pharmgkb | rs2516739 |
| gwascentral | rs2516739 |
| openSNP | rs2516739 |
| 23andMe | rs2516739 |
| SNPshot | rs2516739 |
| SNPdbe | rs2516739 |
| MSV3d | rs2516739 |
| GWAS Ctlg | rs2516739 |
| GMAF | 0.2452 |
| 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 |
