| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Autosomal recessive juvenile Parkinson disease 2 +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive juvenile Parkinson disease 2 +4 more | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive juvenile Parkinson disease 2 +1 more | |
| | LOC126859871, PRKN (S167N) | Single nucleotide variant (missense variant +1 more) | Autosomal recessive juvenile Parkinson disease 2 +4 more | |
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