| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Spinocerebellar ataxia type 1 | |
| | LOC108663993, ATXN1 (Q203H) | Single nucleotide variant (missense variant +1 more) | ATXN1-related disorder +2 more | GConflicting classifications of pathogenicity |
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