| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Spinocerebellar ataxia type 28 +3 more | |
| | | Single nucleotide variant (missense variant) | Optic atrophy 12 +3 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene