| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1 | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa | |
| | | Indel (splice acceptor variant) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
Click to view in NCBI Gene