| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia 47 | |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia 47 +1 more | |
Click to view in NCBI Gene