| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia 47 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
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