"VPS35-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 707481	NM_018206.6(VPS35):c.2145A>G (p.Leu715=)	VPS35	Single nucleotide variant (synonymous variant)	VPS35-related disorder +2 more	GBenign/Likely benign
Select item 1621519	NM_018206.6(VPS35):c.2122A>C (p.Asn708His)	VPS35 (N708H)	Single nucleotide variant (missense variant)	Parkinson disease 17 +2 more	GBenign/Likely benign
Select item 2634308	NM_018206.6(VPS35):c.1327A>G (p.Asn443Asp)	VPS35 (N443D)	Single nucleotide variant (missense variant)	VPS35-related disorder	GUncertain significance
Select item 3044022	NM_018206.6(VPS35):c.915-4_915-3del	VPS35	Deletion (intron variant)	VPS35-related disorder	GBenign
Select item 3039838	NM_018206.6(VPS35):c.831G>A (p.Gln277=)	VPS35	Single nucleotide variant (synonymous variant)	VPS35-related disorder	GLikely benign
Select item 3032290	NM_018206.6(VPS35):c.265A>T (p.Arg89Trp)	VPS35 (R89W)	Single nucleotide variant (missense variant)	VPS35-related disorder	GUncertain significance
Select item 3035055	NM_018206.6(VPS35):c.103-4G>A	VPS35	Single nucleotide variant (intron variant)	VPS35-related disorder	GLikely benign

ClinVar