"Genome Diagnostics Laboratory, Amsterdam University Medical Center"[s - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 41222	NM_004562.3(PRKN):c.1180G>A (p.Asp394Asn)	PRKN (D394N +2 more)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign/Likely benign
Select item 41221	NM_004562.3(PRKN):c.1138G>C (p.Val380Leu)	PRKN (V380L +2 more)	Single nucleotide variant (missense variant)	Autosomal recessive juvenile Parkinson disease 2 +4 more	GBenign
Select item 444707	NM_004562.3(PRKN):c.919C>T (p.Leu307=)	PRKN	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GLikely benign
Select item 574874	NM_004562.3(PRKN):c.766C>T (p.Arg256Cys)	PRKN (R256C +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 41223	NM_004562.3(PRKN):c.500G>A (p.Ser167Asn)	LOC126859871, PRKN (S167N)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GBenign/Likely benign
Select item 259433	NM_004562.3(PRKN):c.413-20T>C	LOC126859871, PRKN	Single nucleotide variant (intron variant)	not specified +1 more	GBenign

ClinVar