| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Retinal dystrophy +1 more | |
| | | Single nucleotide variant (splice donor variant) | Retinal dystrophy | |
| | | Single nucleotide variant (nonsense) | not provided +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Usher syndrome type 1F +3 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene