| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease, dominant intermediate G +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Charcot-Marie-Tooth disease type 1F | |
Click to view in NCBI Gene