| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Charcot-Marie-Tooth disease type 2D +2 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2D +2 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease type 2D +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Distal spinal muscular atrophy +2 more | |
| | | Single nucleotide variant (synonymous variant) | Distal spinal muscular atrophy +2 more | |
| | | Single nucleotide variant (missense variant) | Neuronopathy, distal hereditary motor, type 5A +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Distal spinal muscular atrophy +2 more | |
| | | Single nucleotide variant | Distal spinal muscular atrophy +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Distal spinal muscular atrophy +2 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Distal spinal muscular atrophy +2 more | |
| | | Single nucleotide variant | Distal spinal muscular atrophy +2 more | |
| | | Single nucleotide variant (missense variant) | Distal spinal muscular atrophy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2D +3 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 | |
| | | Single nucleotide variant (missense variant) | Neuronopathy, distal hereditary motor, type 5 +1 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Neuronopathy, distal hereditary motor, type 5A +3 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Charcot-Marie-Tooth disease type 2D +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Charcot-Marie-Tooth disease type 2D +3 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2D +5 more | |
| | | Single nucleotide variant (synonymous variant) | Distal spinal muscular atrophy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease type 2D +4 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +6 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2D +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Neuronopathy, distal hereditary motor, type 5A +6 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease +6 more | |
| | | Single nucleotide variant (missense variant) | Neuronopathy, distal hereditary motor, type 5A +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Neuronopathy, distal hereditary motor, type 5A +2 more | |
| | | Single nucleotide variant (intron variant) | Neuronopathy, distal hereditary motor, type 5A +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2D +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2D +4 more | |
| | | Single nucleotide variant (synonymous variant) | Neuronopathy, distal hereditary motor, type 5A +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Neuronopathy, distal hereditary motor, type 5A +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease type 2D +6 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease type 2D +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease type 2D +6 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Charcot-Marie-Tooth disease type 2D +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Charcot-Marie-Tooth disease type 2D +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Neuronopathy, distal hereditary motor, type 5A +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Neuronopathy, distal hereditary motor, type 5A +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Distal spinal muscular atrophy +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant | Distal spinal muscular atrophy +2 more | |
| | | Single nucleotide variant | not provided +3 more | |
| | | Single nucleotide variant | not provided +3 more | |
| | | Single nucleotide variant | Distal spinal muscular atrophy +3 more | |
| | | Single nucleotide variant | Neuronopathy, distal hereditary motor, type 5A +2 more | |
| | | Single nucleotide variant | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Neuronopathy, distal hereditary motor, type 5A +6 more | |
| | | Single nucleotide variant (intron variant) | Neuronopathy, distal hereditary motor, type 5A +7 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Neuronopathy, distal hereditary motor, type 5A +7 more | |
| | | Single nucleotide variant (intron variant) | Neuronopathy, distal hereditary motor, type 5A +6 more | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Charcot-Marie-Tooth disease +6 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease type 2 +6 more | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Neuronopathy, distal hereditary motor, type 5A +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2D +6 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Neuronopathy, distal hereditary motor, type 5A +5 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease type 2D +5 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease type 2D +6 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2D +6 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +6 more | |
| | | Single nucleotide variant (intron variant) | Neuronopathy, distal hereditary motor, type 5A +5 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2D +2 more | GConflicting classifications of pathogenicity |