| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia +2 more | |
| | | Single nucleotide variant (synonymous variant) | ALS2-Related Disorders +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Juvenile primary lateral sclerosis +6 more | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia +5 more | |
Click to view in NCBI Gene