| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Retinal dystrophy +3 more | GPathogenic/Likely pathogenic |
| | LOC130066823, CFAP410 (A12fs) | Insertion (frameshift variant) | Retinal dystrophy +2 more | |
Click to view in NCBI Gene