| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion | Autosomal recessive early-onset Parkinson disease 6 | |
| | AADACL3, AADACL4 +207 more | Copy number loss | not provided | |
| | | Deletion (frameshift variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | PINK1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Deletion (frameshift variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Insertion (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Deletion (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Deletion (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Copy number gain | not provided | |
| | LOC112577491, LOC112577504 +2149 more | Copy number gain | Trisomy 12p | |
| | | Single nucleotide variant (missense variant) | Neuroblastoma | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (splice acceptor variant) | PINK1-related disorder | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Deletion | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Deletion | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Duplication | Congenital disorder of glycosylation type Ir +2 more | |
| | | Duplication | Deficiency of hydroxymethylglutaryl-CoA lyase | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Duplication (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (intron variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Duplication (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Indel (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Deletion (frameshift variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive early-onset Parkinson disease 6 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive early-onset Parkinson disease 6 | |