| Approved symbol | SMARCB1 |
|---|---|
| Approved name | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 |
| HGCN ID | HGNC:11103 |
| Previous symbols | SNF5L1 |
| Inheritance | |
| OMIM | 601607 |
| Chromosome | 22q11.23 |
| Panel(s) |
NGS Cornelia de Lange syndrome NGS Hereditary cancer panel 1 NGS Hereditary cancer panel 2 NGS Intellectual disability NGS Mendeliome NGS Skeletal Dysplasia |
