| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (stop lost) | Leber congenital amaurosis 11 +2 more | |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 11 +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene