| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive spastic paraplegia type 78 +2 more | |
| | | Single nucleotide variant (missense variant) | ATP13A2-related disorders +3 more | GConflicting classifications of pathogenicity |
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