| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis | |
| | | Deletion (frameshift variant) | Leber congenital amaurosis 13 +1 more | |
| | | Deletion (frameshift variant) | Leber congenital amaurosis | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis | |
| | | Microsatellite (frameshift variant +2 more) | Leber congenital amaurosis | |
| | | Single nucleotide variant (nonsense) | Leber congenital amaurosis | |
| | | Single nucleotide variant (missense variant +1 more) | Leber congenital amaurosis | |
| | | Indel (missense variant) | Leber congenital amaurosis | |
| | | Single nucleotide variant (splice acceptor variant) | Retinitis pigmentosa 20 +2 more | |
| | | Indel (frameshift variant +1 more) | Leber congenital amaurosis | |
| | | Deletion (frameshift variant) | Leber congenital amaurosis | |
| | | Single nucleotide variant (nonsense +1 more) | Leber congenital amaurosis | |
| | | Single nucleotide variant (nonsense) | Leber congenital amaurosis | |
| | LOC130056226, SPATA7 (M1I) | Single nucleotide variant (missense variant +1 more) | Leber congenital amaurosis | |
| | | Duplication (nonsense) | Leber congenital amaurosis | |
| | | Deletion | Leber congenital amaurosis | |
| | | Deletion (frameshift variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | RPE65-related recessive retinopathy | |
| | | Single nucleotide variant (nonsense) | Leber congenital amaurosis +1 more | |
| | GPHN, RDH12 +1 more (A262fs) | Deletion (frameshift variant) | Leber congenital amaurosis 13 +1 more | |
| | | Single nucleotide variant (splice donor variant) | Leber congenital amaurosis +1 more | |
| | ZFYVE26, RDH12 +1 more (V233D) | Single nucleotide variant (missense variant) | Leber congenital amaurosis | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | |
| | | Single nucleotide variant (missense variant +2 more) | Retinitis pigmentosa 12 +3 more | |
| | | Single nucleotide variant (nonsense) | Leber congenital amaurosis | |
| | | Deletion (frameshift variant) | Leber congenital amaurosis | |
| | | Single nucleotide variant (missense variant) | Alstrom syndrome +1 more | |
| | | Duplication (frameshift variant) | Leber congenital amaurosis | |
| | | Deletion (frameshift variant) | Leber congenital amaurosis | |
| | | Single nucleotide variant (missense variant) | RPE65-related recessive retinopathy | |
| | GPHN, RDH12 +1 more (V223F) | Single nucleotide variant (missense variant) | Retinal dystrophy +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant +1 more) | Leber congenital amaurosis | |
| | | Single nucleotide variant (nonsense +1 more) | Leber congenital amaurosis | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis | |
| | IFT140, LOC126862260 (L945P) | Single nucleotide variant (missense variant) | Retinitis pigmentosa 80 +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Insertion (frameshift variant) | Leber congenital amaurosis | |
| | | Single nucleotide variant (synonymous variant) | Leber congenital amaurosis 2 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Meckel-Gruber syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Retinitis pigmentosa 12 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Meckel-Gruber syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Meckel-Gruber syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Familial aplasia of the vermis +2 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Retinitis pigmentosa 12 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Nephronophthisis +7 more | |
| | | Single nucleotide variant (synonymous variant) | Nephronophthisis +2 more | |
| | | Single nucleotide variant (synonymous variant) | Nephronophthisis +2 more | |
| | | Single nucleotide variant (synonymous variant) | Leber congenital amaurosis 13 | |
| | | Single nucleotide variant (synonymous variant +2 more) | Retinitis pigmentosa 12 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Retinitis pigmentosa 12 +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Retinitis pigmentosa 12 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Meckel-Gruber syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Pigmented paravenous retinochoroidal atrophy +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Leber congenital amaurosis +1 more | |
| | | Duplication (frameshift variant) | Leber congenital amaurosis +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Nephronophthisis +8 more | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 2 +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Retinitis pigmentosa 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Leber congenital amaurosis 13 | |
| | | Single nucleotide variant (splice acceptor variant) | Retinitis pigmentosa 20 +1 more | |
| | | Deletion (frameshift variant) | Leber congenital amaurosis 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Retinitis pigmentosa 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Familial aplasia of the vermis +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Retinitis pigmentosa 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Familial aplasia of the vermis +2 more | |
| | | Single nucleotide variant (missense variant) | Meckel-Gruber syndrome +7 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +9 more | |
| | | Microsatellite (inframe_deletion +1 more) | Familial aplasia of the vermis +2 more | |
| | | Single nucleotide variant (missense variant +2 more) | Retinitis pigmentosa 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 13 | |
| | | Single nucleotide variant (missense variant +2 more) | Retinitis pigmentosa 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Meckel syndrome, type 4 +7 more | |
| | | Single nucleotide variant (missense variant) | Retinitis pigmentosa 20 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Retinitis pigmentosa 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Meckel-Gruber syndrome +2 more | |
| | | Single nucleotide variant (missense variant +2 more) | Retinitis pigmentosa 12 +1 more | |
| | | Microsatellite (inframe_deletion) | Leber congenital amaurosis 13 | |
| | | Single nucleotide variant (missense variant +2 more) | Retinitis pigmentosa 12 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Leber congenital amaurosis 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Meckel-Gruber syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Meckel-Gruber syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 2 +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Retinitis pigmentosa 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Meckel-Gruber syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Meckel-Gruber syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy +3 more | |
| | | Single nucleotide variant (missense variant) | Meckel-Gruber syndrome +7 more | |
| | | Single nucleotide variant (missense variant) | CEP290-related disorder +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Retinitis pigmentosa 12 +2 more | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 2 +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Retinitis pigmentosa 12 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Retinitis pigmentosa 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +9 more | |
| | | Single nucleotide variant (missense variant) | Familial aplasia of the vermis +2 more | |