| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 13 +1 more | |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 13 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | KCNC3, LOC111811967 (G47D) | Single nucleotide variant (missense variant +1 more) | Spinocerebellar ataxia type 13 | |
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