| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (intron variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Neuronopathy, distal hereditary motor, type 7B +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Neuronopathy, distal hereditary motor, type 7B +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Neuronopathy, distal hereditary motor, type 7B +5 more | GConflicting classifications of pathogenicity |
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