| | | Copy number loss | Hereditary liability to pressure palsies | |
| | | Copy number loss | Hereditary liability to pressure palsies | |
| | ADORA2B, ARHGAP44 +18 more | Copy number loss | Hereditary liability to pressure palsies | |
| | | Copy number loss | Hereditary liability to pressure palsies | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary liability to pressure palsies | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary liability to pressure palsies +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease, type I +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary liability to pressure palsies +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Hereditary liability to pressure palsies +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +6 more | |
| | | Single nucleotide variant (intron variant) | Hereditary liability to pressure palsies | |
| | | Deletion (frameshift variant +1 more) | Charcot-Marie-Tooth disease | |
| | | Single nucleotide variant (missense variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (nonsense +1 more) | Charcot-Marie-Tooth disease, type I | |
| | | Single nucleotide variant (nonsense +1 more) | Hereditary liability to pressure palsies | |
| | | Duplication (frameshift variant +1 more) | Hereditary liability to pressure palsies | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Guillain-Barre syndrome, familial +5 more | |
| | | Copy number loss | Hereditary liability to pressure palsies | |
| | | Copy number loss | Hereditary liability to pressure palsies | |
| | | Copy number loss | Hereditary liability to pressure palsies | |
| | | Copy number loss | Hereditary liability to pressure palsies | |
| | | Copy number loss | Hereditary liability to pressure palsies | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | Charcot-Marie-Tooth disease, type I +6 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease, type I +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Charcot-Marie-Tooth disease, type I +9 more | |
| | | Single nucleotide variant | Hereditary liability to pressure palsies +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +9 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +3 more | |
| | | Microsatellite (3 prime UTR variant +1 more) | Hereditary liability to pressure palsies +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Microsatellite (3 prime UTR variant +1 more) | Hereditary liability to pressure palsies +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Hereditary liability to pressure palsies +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Hereditary liability to pressure palsies +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Hereditary liability to pressure palsies +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Charcot-Marie-Tooth disease, type I +1 more | |
| | | Single nucleotide variant (synonymous variant) | Thyrotoxic periodic paralysis, susceptibility to, 1 +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary liability to pressure palsies +8 more | |
| | | Single nucleotide variant (missense variant) | Hereditary liability to pressure palsies | |
| | | Deletion | Autosomal recessive Dejerine-Sottas syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease, type IA +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Charcot-Marie-Tooth disease, type I +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Charcot-Marie-Tooth disease, type I +2 more | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant +1 more) | Charcot-Marie-Tooth disease, type I +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Charcot-Marie-Tooth disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Charcot-Marie-Tooth disease, type IA +5 more | GConflicting classifications of pathogenicity |
| | | Deletion | Hereditary liability to pressure palsies +2 more | |