rs146170505
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs146170505(A;A) |
| Make rs146170505(A;C) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 1 |
| Position | 97699370 |
| Gene | DPYD |
| is a | snp |
| is | mentioned by |
| dbSNP | rs146170505 |
| dbSNP (classic) | rs146170505 |
| ClinGen | rs146170505 |
| ebi | rs146170505 |
| HLI | rs146170505 |
| Exac | rs146170505 |
| Gnomad | rs146170505 |
| Varsome | rs146170505 |
| LitVar | rs146170505 |
| Map | rs146170505 |
| PheGenI | rs146170505 |
| Biobank | rs146170505 |
| 1000 genomes | rs146170505 |
| hgdp | rs146170505 |
| ensembl | rs146170505 |
| geneview | rs146170505 |
| scholar | rs146170505 |
| rs146170505 | |
| pharmgkb | rs146170505 |
| gwascentral | rs146170505 |
| openSNP | rs146170505 |
| 23andMe | rs146170505 |
| SNPshot | rs146170505 |
| SNPdbe | rs146170505 |
| MSV3d | rs146170505 |
| GWAS Ctlg | rs146170505 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs146170505(A;A) |
| Alt | rs146170505(A;A) |
| Reference | Rs146170505(C;C) |
| Significance | Probable-Pathogenic |
| Disease | Dihydropyrimidine dehydrogenase deficiency |
| Variation | info |
| Gene | DPYD |
| CLNDBN | Dihydropyrimidine dehydrogenase deficiency |
| Reversed | 0 |
| HGVS | NC_000001.10:g.98164926C>A |
| CLNSRC | |
| CLNACC | RCV000410667.1, |
