| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (nonsense +1 more) | Retinitis pigmentosa 26 +1 more | GPathogenic/Likely pathogenic |
| | CERKL, LOC129935215 (W3fs) | Deletion (frameshift variant +1 more) | Retinitis pigmentosa 26 | |
Click to view in NCBI Gene