| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Autosomal dominant Parkinson disease 8 | |
| | | Single nucleotide variant (nonsense) | Autosomal dominant Parkinson disease 8 | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant Parkinson disease 8 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Autosomal dominant Parkinson disease 8 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant Parkinson disease 8 | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant Parkinson disease 8 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal dominant Parkinson disease 8 | |
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