| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (intron variant) | Congenital Stationary Night Blindness, Dominant +2 more | |
| | | Deletion (3 prime UTR variant) | Retinitis Pigmentosa, Dominant/Recessive +1 more | |
| | | Deletion (3 prime UTR variant) | Congenital Stationary Night Blindness, Dominant +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Retinitis Pigmentosa, Dominant/Recessive +1 more | |
Click to view in NCBI Gene