| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Parkinsonism-dystonia, infantile, 2 +1 more | |
| | SLC18A2, SLC18A2-AS1 (W11*) | Single nucleotide variant (nonsense) | not provided | |
| | SLC18A2, SLC18A2-AS1 (D33A) | Single nucleotide variant (missense variant) | not provided | |
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