| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Retinal dystrophy +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Joubert syndrome 23 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
Click to view in NCBI Gene