| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Neuronopathy, distal hereditary motor, type 5B +6 more | GConflicting classifications of pathogenicity |
| | | Indel (missense variant +1 more) | Hereditary spastic paraplegia 31 | |
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