| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Cone-rod dystrophy 13 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cone-rod dystrophy 13 +1 more | |
| | | Deletion (frameshift variant) | Leber congenital amaurosis 6 | |
Click to view in NCBI Gene