"PRKN-related disorder"[Disease/phenotype] AND "PreventionGenetics, pa - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 356011	NM_004562.3(PRKN):c.*108AC[5]	PRKN	Microsatellite (3 prime UTR variant)	PRKN-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 356016	NM_004562.3(PRKN):c.1289G>A (p.Gly430Asp)	PRKN (G430D +2 more)	Single nucleotide variant (missense variant)	not provided +5 more	GPathogenic/Likely pathogenic
Select item 415532	NM_004562.3(PRKN):c.957T>C (p.Gly319=)	PRKN	Single nucleotide variant (synonymous variant)	PRKN-related disorder +2 more	GBenign/Likely benign
Select item 7050	NM_004562.3(PRKN):c.823C>T (p.Arg275Trp)	PRKN (R275W +2 more)	Single nucleotide variant (missense variant)	See cases +7 more	GPathogenic
Select item 578186	NM_004562.3(PRKN):c.98G>A (p.Arg33Gln)	PRKN (R33Q)	Single nucleotide variant (missense variant)	not provided +4 more	GPathogenic/Likely pathogenic
Select item 1128762	NM_004562.3(PRKN):c.51C>T (p.Val17=)	PRKN	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 356022	NM_004562.3(PRKN):c.-30T>C	PACRG, PRKN	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +2 more	GBenign/Likely benign

ClinVar