| Approved symbol | SF3B2 |
|---|---|
| Approved name | splicing factor 3b subunit 2 |
| HGCN ID | HGNC:10769 |
| Previous symbols | |
| Inheritance | |
| OMIM | 605591 |
| Chromosome | 11q13.1 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
