rs202037973
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs202037973(A;G) |
| Make rs202037973(G;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 15 |
| Position | 89323423 |
| Gene | POLG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs202037973 |
| dbSNP (classic) | rs202037973 |
| ClinGen | rs202037973 |
| ebi | rs202037973 |
| HLI | rs202037973 |
| Exac | rs202037973 |
| Gnomad | rs202037973 |
| Varsome | rs202037973 |
| LitVar | rs202037973 |
| Map | rs202037973 |
| PheGenI | rs202037973 |
| Biobank | rs202037973 |
| 1000 genomes | rs202037973 |
| hgdp | rs202037973 |
| ensembl | rs202037973 |
| geneview | rs202037973 |
| scholar | rs202037973 |
| rs202037973 | |
| pharmgkb | rs202037973 |
| gwascentral | rs202037973 |
| openSNP | rs202037973 |
| 23andMe | rs202037973 |
| SNPshot | rs202037973 |
| SNPdbe | rs202037973 |
| MSV3d | rs202037973 |
| GWAS Ctlg | rs202037973 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs202037973(G;G) |
| Alt | rs202037973(G;G) |
| Reference | Rs202037973(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided not specified |
| Variation | info |
| Gene | POLG |
| CLNDBN | not provided not specified |
| Reversed | 0 |
| HGVS | NC_000015.9:g.89866654A>G |
| CLNSRC | |
| CLNACC | RCV000188572.3, RCV000275508.1, |
