rs35706870
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs35706870(A;A) |
| Make rs35706870(A;C) |
| Make rs35706870(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 67883859 |
| Gene | SIRT1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35706870 |
| dbSNP (classic) | rs35706870 |
| ClinGen | rs35706870 |
| ebi | rs35706870 |
| HLI | rs35706870 |
| Exac | rs35706870 |
| Gnomad | rs35706870 |
| Varsome | rs35706870 |
| LitVar | rs35706870 |
| Map | rs35706870 |
| PheGenI | rs35706870 |
| Biobank | rs35706870 |
| 1000 genomes | rs35706870 |
| hgdp | rs35706870 |
| ensembl | rs35706870 |
| geneview | rs35706870 |
| scholar | rs35706870 |
| rs35706870 | |
| pharmgkb | rs35706870 |
| gwascentral | rs35706870 |
| openSNP | rs35706870 |
| 23andMe | rs35706870 |
| SNPshot | rs35706870 |
| SNPdbe | rs35706870 |
| MSV3d | rs35706870 |
| GWAS Ctlg | rs35706870 |
| Max Magnitude | 0 |
[PMID 24875419] Functional sequence variants within the SIRT1 gene promoter in indirect inguinal hernia
