C3160718[trait identifier] AND "Neurogenetic Laboratory, Oslo Universi - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 96726	NM_007262.5(PARK7):c.399G>C (p.Met133Ile)	PARK7 (M133I)	Single nucleotide variant (missense variant)	Parkinson disease, late-onset	GUncertain significance
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
Select item 96730	NM_198578.4(LRRK2):c.2352C>A (p.Ser784Arg)	LRRK2 (S784R)	Single nucleotide variant (missense variant)	Autosomal dominant Parkinson disease 8	GUncertain significance
Select item 96731	NM_198578.4(LRRK2):c.7300A>G (p.Ile2434Val)	LRRK2 (I2434V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 96727	NM_018206.6(VPS35):c.1576C>T (p.Arg526Cys)	VPS35 (R526C)	Single nucleotide variant (missense variant)	Parkinson disease, late-onset	GUncertain significance

ClinVar