rs74853476
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs74853476(C;C) |
| Make rs74853476(C;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 9 |
| Position | 133636712 |
| Gene | DBH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs74853476 |
| dbSNP (classic) | rs74853476 |
| ClinGen | rs74853476 |
| ebi | rs74853476 |
| HLI | rs74853476 |
| Exac | rs74853476 |
| Gnomad | rs74853476 |
| Varsome | rs74853476 |
| LitVar | rs74853476 |
| Map | rs74853476 |
| PheGenI | rs74853476 |
| Biobank | rs74853476 |
| 1000 genomes | rs74853476 |
| hgdp | rs74853476 |
| ensembl | rs74853476 |
| geneview | rs74853476 |
| scholar | rs74853476 |
| rs74853476 | |
| pharmgkb | rs74853476 |
| gwascentral | rs74853476 |
| openSNP | rs74853476 |
| 23andMe | rs74853476 |
| SNPshot | rs74853476 |
| SNPdbe | rs74853476 |
| MSV3d | rs74853476 |
| GWAS Ctlg | rs74853476 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs74853476(C;C) |
| Alt | rs74853476(C;C) |
| Reference | Rs74853476(T;T) |
| Significance | Pathogenic |
| Disease | Dopamine beta hydroxylase deficiency not provided |
| Variation | info |
| Gene | DBH |
| CLNDBN | Dopamine beta hydroxylase deficiency not provided |
| Reversed | 0 |
| HGVS | NC_000009.11:g.136501834T>C |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000001820.5, RCV000486465.1, |
