| Approved symbol | SAMD9L |
|---|---|
| Approved name | sterile alpha motif domain containing 9 like |
| HGCN ID | HGNC:1349 |
| Previous symbols | C7orf6 |
| Inheritance | |
| OMIM | 611170 |
| Chromosome | 7q21.2 |
| Panel(s) |
NGS Dementia/ALS NGS Mendeliome NGS Movement disorders NGS Primary immunodeficiency PID NGS White matter disease |
