| Approved symbol | INVS |
|---|---|
| Approved name | inversin |
| HGCN ID | HGNC:17870 |
| Previous symbols | NPHP2 |
| Inheritance | |
| OMIM | 243305 |
| Chromosome | 9q31.1 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB |
