| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Charcot-Marie-Tooth Disease, axonal, type 2GG +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Charcot-Marie-Tooth Disease, axonal, type 2GG +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense +1 more) | Charcot-Marie-Tooth Disease, axonal, type 2GG +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Charcot-Marie-Tooth Disease, axonal, type 2GG +1 more | GPathogenic/Likely pathogenic |
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