| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | LOC130055387, NRL (C219fs +1 more) | Deletion (frameshift variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Retinitis pigmentosa +1 more | |
Click to view in NCBI Gene