| | | Single nucleotide variant (missense variant) | Pigmentary retinal dystrophy +1 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 7 | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 7 | |
| | | Single nucleotide variant (nonsense) | Patterned macular dystrophy 1 +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 7 | |
| | | Deletion (frameshift variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cone-rod dystrophy +9 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 7 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy +4 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Adult-onset foveomacular vitelliform dystrophy +8 more | |
| | | Single nucleotide variant (missense variant) | Adult-onset foveomacular vitelliform dystrophy +10 more | |
| | | Single nucleotide variant (missense variant) | Adult-onset foveomacular vitelliform dystrophy +11 more | |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy +10 more | |
| | | Deletion (frameshift variant) | PRPH2-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 7 +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (inframe_deletion) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Retinitis pigmentosa +10 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 7 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Choroidal dystrophy, central areolar 2 +6 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (inframe_deletion) | PRPH2-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 7 +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Patterned dystrophy of the retinal pigment epithelium +4 more | |
| | | Microsatellite (inframe_deletion) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant) | Retinitis pigmentosa 7 +3 more | GConflicting classifications of pathogenicity |