"Neurogenetic Laboratory, Oslo University Hospital"[submitter] AND "PI - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 96728	NM_032409.3(PINK1):c.644C>T (p.Pro215Leu)	PINK1 (P215L)	Single nucleotide variant (missense variant)	Parkinson disease, late-onset	GUncertain significance
Select item 96729	NM_032409.3(PINK1):c.923T>A (p.Leu308Gln)	PINK1, PINK1-AS (L308Q)	Single nucleotide variant (missense variant)	Parkinson disease, late-onset	GUncertain significance