| Approved symbol | OR2W3 |
|---|---|
| Approved name | olfactory receptor family 2 subfamily W member 3 |
| HGCN ID | HGNC:15021 |
| Previous symbols | OR2W8P, OR2W3P |
| Inheritance | |
| OMIM | 616729 |
| Chromosome | 1q44 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Retinitis pigmentosa NGS Vision disorder CSNB |
