| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 10 +3 more | |
| | | Single nucleotide variant (intron variant) | Spastic paraplegia +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | Spastic paraplegia +3 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene