rs775538075
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs775538075(A;G) |
| Make rs775538075(G;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 15 |
| Position | 89327300 |
| Gene | MIR6766, POLG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs775538075 |
| dbSNP (classic) | rs775538075 |
| ClinGen | rs775538075 |
| ebi | rs775538075 |
| HLI | rs775538075 |
| Exac | rs775538075 |
| Gnomad | rs775538075 |
| Varsome | rs775538075 |
| LitVar | rs775538075 |
| Map | rs775538075 |
| PheGenI | rs775538075 |
| Biobank | rs775538075 |
| 1000 genomes | rs775538075 |
| hgdp | rs775538075 |
| ensembl | rs775538075 |
| geneview | rs775538075 |
| scholar | rs775538075 |
| rs775538075 | |
| pharmgkb | rs775538075 |
| gwascentral | rs775538075 |
| openSNP | rs775538075 |
| 23andMe | rs775538075 |
| SNPshot | rs775538075 |
| SNPdbe | rs775538075 |
| MSV3d | rs775538075 |
| GWAS Ctlg | rs775538075 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs775538075(G;G) |
| Alt | rs775538075(G;G) |
| Reference | Rs775538075(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | MIR6766 POLG |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000015.9:g.89870531A>G |
| CLNSRC | |
| CLNACC | RCV000188654.1, |
