| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Charcot-Marie-Tooth Neuropathy X +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth Neuropathy X +1 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Charcot-Marie-Tooth disease X-linked dominant 1 | |
Click to view in NCBI Gene