List of variants reported as uncertain significance for Juvenile-onset Parkinson disease by Illumina Laboratory Services, Illumina

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

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_004562.2(PRKN):c.-107G>A	rs886061239	0.00020
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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