| Approved symbol | RS1 |
|---|---|
| Approved name | retinoschisin 1 |
| HGCN ID | HGNC:10457 |
| Previous symbols | RS |
| Inheritance | |
| OMIM | 300839 |
| Chromosome | Xp22.13 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB RS1 Analysis |
