| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Deletion (intron variant) | Parkinson Disease, Dominant +3 more | |
| | | Single nucleotide variant (synonymous variant) | Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Parkinson disease 5, autosomal dominant, susceptibility to +1 more | |
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