| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Copy number gain | See cases | |
| | | Deletion (frameshift variant) | Autosomal dominant cerebellar ataxia | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | MYRF-related disorder | |
| | | Single nucleotide variant (intron variant) | not provided | |
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