| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia +4 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia +4 more | |
| | FA2H, LOC130059394 (P44fs) | Deletion (frameshift variant) | Hereditary spastic paraplegia 35 | |
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