| | | Single nucleotide variant (nonsense) | Usher syndrome type 2A +2 more | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | |
| | | Microsatellite (frameshift variant) | Usher syndrome type 2A +3 more | |
| | | Single nucleotide variant (nonsense) | Usher syndrome type 3A +10 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 39 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Usher syndrome type 2A +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 39 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Usher syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 39 +6 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Rare genetic deafness +22 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Usher syndrome | |
| | | Single nucleotide variant (splice acceptor variant) | Retinitis pigmentosa +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | not provided +2 more | |
| | | Deletion (frameshift variant) | Retinal dystrophy +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cone-rod dystrophy 3 | |