rs148597698
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs148597698(A;A) |
| Make rs148597698(A;C) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 17 |
| Position | 47945914 |
| Gene | PNPO |
| is a | snp |
| is | mentioned by |
| dbSNP | rs148597698 |
| dbSNP (classic) | rs148597698 |
| ClinGen | rs148597698 |
| ebi | rs148597698 |
| HLI | rs148597698 |
| Exac | rs148597698 |
| Gnomad | rs148597698 |
| Varsome | rs148597698 |
| LitVar | rs148597698 |
| Map | rs148597698 |
| PheGenI | rs148597698 |
| Biobank | rs148597698 |
| 1000 genomes | rs148597698 |
| hgdp | rs148597698 |
| ensembl | rs148597698 |
| geneview | rs148597698 |
| scholar | rs148597698 |
| rs148597698 | |
| pharmgkb | rs148597698 |
| gwascentral | rs148597698 |
| openSNP | rs148597698 |
| 23andMe | rs148597698 |
| SNPshot | rs148597698 |
| SNPdbe | rs148597698 |
| MSV3d | rs148597698 |
| GWAS Ctlg | rs148597698 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs148597698(A;A) |
| Alt | rs148597698(A;A) |
| Reference | Rs148597698(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | PNPO |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.46023280C>A |
| CLNSRC | |
| CLNACC | RCV000188490.1, |
