| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC101927157, CNGA1 (R420Q) | Single nucleotide variant (missense variant) | Retinitis pigmentosa +2 more | GConflicting classifications of pathogenicity |
| | CNGA1, LOC101927157 (L85fs) | Deletion (frameshift variant) | Retinitis pigmentosa 49 +3 more | |
| | CNGA1, LOC101927157 (G60fs) | Deletion (frameshift variant) | not provided +1 more | |
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