| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | Neuronopathy, distal hereditary motor, type 2A +1 more | |
| | | Single nucleotide variant | Charcot-Marie-Tooth disease axonal type 2L +1 more | |
| | | Single nucleotide variant | Charcot-Marie-Tooth disease axonal type 2L +1 more | |
| | | Single nucleotide variant | Charcot-Marie-Tooth disease axonal type 2L +1 more | |
| | | Single nucleotide variant | Neuronopathy, distal hereditary motor, type 2A +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Charcot-Marie-Tooth disease axonal type 2L +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Charcot-Marie-Tooth disease axonal type 2L +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Charcot-Marie-Tooth disease axonal type 2L +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Charcot-Marie-Tooth disease axonal type 2L +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Indel (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L +2 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L +1 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (nonsense) | Charcot-Marie-Tooth disease axonal type 2L +1 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L +1 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L +1 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L +1 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2L | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease axonal type 2L | |