rs769637557
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs769637557(G;G) |
| Make rs769637557(G;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 15 |
| Position | 89327004 |
| Gene | MIR6766, POLG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs769637557 |
| dbSNP (classic) | rs769637557 |
| ClinGen | rs769637557 |
| ebi | rs769637557 |
| HLI | rs769637557 |
| Exac | rs769637557 |
| Gnomad | rs769637557 |
| Varsome | rs769637557 |
| LitVar | rs769637557 |
| Map | rs769637557 |
| PheGenI | rs769637557 |
| Biobank | rs769637557 |
| 1000 genomes | rs769637557 |
| hgdp | rs769637557 |
| ensembl | rs769637557 |
| geneview | rs769637557 |
| scholar | rs769637557 |
| rs769637557 | |
| pharmgkb | rs769637557 |
| gwascentral | rs769637557 |
| openSNP | rs769637557 |
| 23andMe | rs769637557 |
| SNPshot | rs769637557 |
| SNPdbe | rs769637557 |
| MSV3d | rs769637557 |
| GWAS Ctlg | rs769637557 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs769637557(G;G) |
| Alt | rs769637557(G;G) |
| Reference | Rs769637557(T;T) |
| Significance | Probable-Pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | MIR6766 POLG |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000015.9:g.89870235T>G |
| CLNSRC | |
| CLNACC | RCV000188661.2, |
