| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Leber congenital amaurosis 7 +4 more | |
| | | Duplication (frameshift variant) | Cone-rod dystrophy 2 | |
Click to view in NCBI Gene