| | | Single nucleotide variant (missense variant +1 more) | Leber congenital amaurosis 15 | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 15 | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 15 | |
| | | Single nucleotide variant (nonsense) | Leber congenital amaurosis +1 more | |
| | | Single nucleotide variant (intron variant) | Leber congenital amaurosis 15 | |
| | | Single nucleotide variant (intron variant) | Leber congenital amaurosis 15 +2 more | |
| | | Single nucleotide variant (intron variant) | Leber congenital amaurosis 15 +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 14 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 15 | |
| | | Deletion (frameshift variant) | Leber congenital amaurosis 15 | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Leber congenital amaurosis 15 | |
| | | Single nucleotide variant (splice donor variant) | Leber congenital amaurosis 15 | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 15 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 15 | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 15 +2 more | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 15 +1 more | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 15 +2 more | |
| | | Single nucleotide variant (intron variant) | Leber congenital amaurosis 15 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Retinitis pigmentosa +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Leber congenital amaurosis 15 +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Leber congenital amaurosis 15 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Retinitis pigmentosa +3 more | |
| | | Deletion (frameshift variant) | Leber congenital amaurosis 15 | |
| | | Single nucleotide variant (nonsense) | Abnormality of the eye +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Leber congenital amaurosis 15 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 15 +1 more | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 15 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Leber congenital amaurosis 15 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Leber congenital amaurosis 15 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa +3 more | |
| | | Single nucleotide variant (intron variant) | Leber congenital amaurosis 15 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 15 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 15 +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis pigmentosa +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Leber congenital amaurosis 15 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Leber congenital amaurosis 15 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Leber congenital amaurosis 15 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Leber congenital amaurosis 15 +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Leber congenital amaurosis 15 +5 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (splice donor variant) | Retinitis pigmentosa 14 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy +6 more | |
| | | Single nucleotide variant (intron variant) | Retinitis pigmentosa 14 +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice donor variant) | Retinitis pigmentosa 14 +3 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +6 more | |
| | | Duplication (inframe_insertion) | Leber congenital amaurosis 15 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Brachydactyly +4 more | |
| | | Single nucleotide variant (nonsense) | Leber congenital amaurosis 15 | |
| | | Deletion (frameshift variant) | not provided +1 more | |