| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cone-rod dystrophy 12 +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Cone-rod dystrophy 12 +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +4 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cone-rod dystrophy 12 +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cone-rod dystrophy 12 +3 more | |
| | | Single nucleotide variant (intron variant) | Retinitis pigmentosa +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Cone-rod dystrophy 12 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Retinal dystrophy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (intron variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinal macular dystrophy type 2 +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cone-rod dystrophy 12 +3 more | |
| | | Single nucleotide variant (intron variant) | not specified +6 more | |
| | | Single nucleotide variant (intron variant) | Stargardt disease 4 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Retinitis pigmentosa +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cone-rod dystrophy 12 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Retinitis pigmentosa +4 more | |
| | | Single nucleotide variant (intron variant) | not specified +6 more | |
| | | Single nucleotide variant (synonymous variant) | Retinitis pigmentosa +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Retinitis pigmentosa +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cone-rod dystrophy 12 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (intron variant) | Retinitis pigmentosa +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Stargardt disease 4 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (intron variant) | not specified +5 more | |
| | | Single nucleotide variant (missense variant) | PROM1-related condition +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | Retinal dystrophy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Stargardt disease 4 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Retinitis pigmentosa +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cone-rod dystrophy 12 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Stargardt disease 4 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinal macular dystrophy type 2 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | PROM1-related condition +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cone-rod dystrophy 12 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cone-rod dystrophy 12 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Stargardt disease 4 +4 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (synonymous variant) | Cone-rod dystrophy 12 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +4 more | |
| | | Single nucleotide variant (intron variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (missense variant) | Cone-rod dystrophy 12 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Retinitis pigmentosa +6 more | |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Stargardt disease 4 +4 more | |
| | | Single nucleotide variant (synonymous variant) | Stargardt disease 4 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Retinal dystrophy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Retinitis pigmentosa +5 more | |
| | | Single nucleotide variant (missense variant) | Cone-rod dystrophy 12 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Retinitis pigmentosa +6 more | |
| | | Single nucleotide variant (intron variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Retinitis pigmentosa +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (synonymous variant) | Retinal dystrophy +6 more | |
| | | Single nucleotide variant (missense variant) | Stargardt disease 4 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cone-rod dystrophy 12 +4 more | |