List of variants in gene PRKN reported as uncertain significance for Juvenile-onset Parkinson disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_004562.3(PRKN):c.*1024TC[2]	rs886061233
NM_004562.3(PRKN):c.*108AC[5]	rs575581029
NM_004562.3(PRKN):c.*2363C>A	rs12215447
NM_004562.3(PRKN):c.*2524CA[1]	rs761920927
NM_004562.3(PRKN):c.887_890del	rs572345942

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