| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 10 +3 more | |
| | | Single nucleotide variant (intron variant) | Amyotrophic lateral sclerosis, susceptibility to, 25 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Amyotrophic lateral sclerosis, susceptibility to, 25 +6 more | |
| | | Single nucleotide variant (missense variant) | Spastic paraplegia +3 more | GConflicting classifications of pathogenicity |
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