| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Neuronopathy, distal hereditary motor, autosomal recessive 5 +1 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease +3 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
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