rs34928857
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs34928857(C;C) |
| Make rs34928857(C;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 2 |
| Position | 55673071 |
| Gene | PNPT1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34928857 |
| dbSNP (classic) | rs34928857 |
| ClinGen | rs34928857 |
| ebi | rs34928857 |
| HLI | rs34928857 |
| Exac | rs34928857 |
| Gnomad | rs34928857 |
| Varsome | rs34928857 |
| LitVar | rs34928857 |
| Map | rs34928857 |
| PheGenI | rs34928857 |
| Biobank | rs34928857 |
| 1000 genomes | rs34928857 |
| hgdp | rs34928857 |
| ensembl | rs34928857 |
| geneview | rs34928857 |
| scholar | rs34928857 |
| rs34928857 | |
| pharmgkb | rs34928857 |
| gwascentral | rs34928857 |
| openSNP | rs34928857 |
| 23andMe | rs34928857 |
| SNPshot | rs34928857 |
| SNPdbe | rs34928857 |
| MSV3d | rs34928857 |
| GWAS Ctlg | rs34928857 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs34928857(C;C) |
| Alt | rs34928857(C;C) |
| Reference | Rs34928857(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | PNPT1 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000002.11:g.55900206C>G |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000199246.3, |
