rs760270633
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs760270633(C;T) |
| Make rs760270633(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 9 |
| Position | 128220201 |
| Gene | DNM1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs760270633 |
| dbSNP (classic) | rs760270633 |
| ClinGen | rs760270633 |
| ebi | rs760270633 |
| HLI | rs760270633 |
| Exac | rs760270633 |
| Gnomad | rs760270633 |
| Varsome | rs760270633 |
| LitVar | rs760270633 |
| Map | rs760270633 |
| PheGenI | rs760270633 |
| Biobank | rs760270633 |
| 1000 genomes | rs760270633 |
| hgdp | rs760270633 |
| ensembl | rs760270633 |
| geneview | rs760270633 |
| scholar | rs760270633 |
| rs760270633 | |
| pharmgkb | rs760270633 |
| gwascentral | rs760270633 |
| openSNP | rs760270633 |
| 23andMe | rs760270633 |
| SNPshot | rs760270633 |
| SNPdbe | rs760270633 |
| MSV3d | rs760270633 |
| GWAS Ctlg | rs760270633 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs760270633(T;T) |
| Alt | rs760270633(T;T) |
| Reference | Rs760270633(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | DNM1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000009.11:g.130982480C>T |
| CLNSRC | |
| CLNACC | RCV000263789.1, |
