| | | Single nucleotide variant (non-coding transcript variant) | Developmental cataract +1 more | |
| | | Single nucleotide variant (non-coding transcript variant) | Developmental cataract +1 more | |
| | | Single nucleotide variant | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant | Developmental cataract +1 more | |
| | | Single nucleotide variant | Developmental cataract +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (intron variant) | Cataract 38 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Sengers syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Sengers syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Cataract 38 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (intron variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (missense variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | AGK-related condition +3 more | |
| | | Single nucleotide variant (intron variant) | Sengers syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (missense variant) | Cataract 38 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Sengers syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cataract 38 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Cataract 38 +2 more | |
| | | Single nucleotide variant (missense variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (missense variant) | Sengers syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cataract 38 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cataract 38 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Sengers syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cataract 38 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cataract 38 +2 more | |
| | | Single nucleotide variant (missense variant) | Cataract 38 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cataract 38 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Sengers syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Deletion (3 prime UTR variant) | Sengers syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Sengers syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Sengers syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Deletion (3 prime UTR variant) | Developmental cataract +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Microsatellite (3 prime UTR variant) | Sengers syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Duplication (3 prime UTR variant) | Sengers syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Deletion (3 prime UTR variant) | Sengers syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Deletion (3 prime UTR variant) | Sengers syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |
| | | Deletion (3 prime UTR variant) | Sengers syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cataract 38 +1 more | |