| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Cone-rod dystrophy 13 +2 more | |
| | | Single nucleotide variant (splice donor variant) | Leber congenital amaurosis 6 | |
| | | Deletion (splice acceptor variant) | Cone-rod dystrophy 13 +2 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene