| | | Single nucleotide variant (nonsense) | Charcot-Marie-Tooth disease type 4C | |
| | | Deletion (frameshift variant) | Charcot-Marie-Tooth disease type 4C | |
| | | Single nucleotide variant (nonsense) | Susceptibility to mononeuropathy of the median nerve, mild +4 more | |
| | | Single nucleotide variant (nonsense) | Charcot-Marie-Tooth disease type 4 +8 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Charcot-Marie-Tooth disease type 4 +2 more | |
| | | Single nucleotide variant (nonsense) | Charcot-Marie-Tooth disease type 4 +2 more | |
| | | Microsatellite (frameshift variant) | Charcot-Marie-Tooth disease type 4 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Susceptibility to mononeuropathy of the median nerve, mild +2 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (frameshift variant) | Charcot-Marie-Tooth disease type 4C | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant) | Charcot-Marie-Tooth disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 4 +13 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Charcot-Marie-Tooth disease | |