| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Achromatopsia 3 +2 more | |
| | | Single nucleotide variant (missense variant) | Achromatopsia 3 +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (splice acceptor variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Achromatopsia 3 +2 more | |
| | | Single nucleotide variant (splice acceptor variant) | Achromatopsia 3 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice donor variant) | Achromatopsia 3 +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | CNGB3-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Achromatopsia 3 +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice acceptor variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Achromatopsia 3 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene