| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | Neuropathy, hereditary sensory, type 1D +3 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 3A +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Deletion (splice donor variant) | Hereditary spastic paraplegia 3A +1 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +5 more | |
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