| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | Retinitis pigmentosa +2 more | |
| | NRL, LOC130055387 (C219fs +1 more) | Deletion (frameshift variant) | Retinitis pigmentosa 27 +3 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene