rs768653086
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs768653086(C;T) |
| Make rs768653086(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 15 |
| Position | 89320917 |
| Gene | POLG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs768653086 |
| dbSNP (classic) | rs768653086 |
| ClinGen | rs768653086 |
| ebi | rs768653086 |
| HLI | rs768653086 |
| Exac | rs768653086 |
| Gnomad | rs768653086 |
| Varsome | rs768653086 |
| LitVar | rs768653086 |
| Map | rs768653086 |
| PheGenI | rs768653086 |
| Biobank | rs768653086 |
| 1000 genomes | rs768653086 |
| hgdp | rs768653086 |
| ensembl | rs768653086 |
| geneview | rs768653086 |
| scholar | rs768653086 |
| rs768653086 | |
| pharmgkb | rs768653086 |
| gwascentral | rs768653086 |
| openSNP | rs768653086 |
| 23andMe | rs768653086 |
| SNPshot | rs768653086 |
| SNPdbe | rs768653086 |
| MSV3d | rs768653086 |
| GWAS Ctlg | rs768653086 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs768653086(T;T) |
| Alt | rs768653086(T;T) |
| Reference | Rs768653086(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | POLG |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000015.9:g.89864148C>T |
| CLNSRC | |
| CLNACC | RCV000188589.2, |
