| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Autosomal recessive complex spastic paraplegia type 9B | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive complex spastic paraplegia type 9B | |
| | | Single nucleotide variant (missense variant +1 more) | Cutis laxa, autosomal dominant 3 +4 more | |
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