| | | Single nucleotide variant (3 prime UTR variant +1 more) | Hereditary spastic paraplegia +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Spastic paraplegia +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary spastic paraplegia | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary spastic paraplegia | |
| | | Single nucleotide variant (missense variant +1 more) | Spastic paraplegia +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Spastic paraplegia +1 more | |
| | | Single nucleotide variant (missense variant) | Spastic paraplegia +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Spastic paraplegia +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | CYP7B1-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (nonsense) | Spastic paraplegia +3 more | |
| | | Duplication (frameshift variant) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Spastic paraplegia +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 5A +4 more | |
| | | Single nucleotide variant (nonsense) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant) | Hereditary spastic paraplegia 5A +1 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (inframe_deletion) | Hereditary spastic paraplegia | |
| | | Duplication (intron variant) | Spastic paraplegia +3 more | GConflicting classifications of pathogenicity |
| | | Deletion (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | CYP7B1-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Spastic paraplegia +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 5A +4 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +1 more | |