List of variants reported as likely pathogenic for Young-onset Parkinson disease by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_004562.3(PRKN):c.1289G>A (p.Gly430Asp)	rs191486604	0.00013
NM_020821.3(VPS13C):c.1111C>T (p.Arg371Ter)	rs752457309	0.00002
NM_020821.3(VPS13C):c.1119G>A (p.Trp373Ter)	rs2046893100
NM_020821.3(VPS13C):c.2408+1G>A
NM_020821.3(VPS13C):c.3331G>T (p.Gly1111Ter)
NM_020821.3(VPS13C):c.3908+2T>C
NM_020821.3(VPS13C):c.4165G>C (p.Gly1389Arg)	rs369100678
NM_020821.3(VPS13C):c.5462T>A (p.Leu1821Ter)
NM_020821.3(VPS13C):c.5698C>T (p.Gln1900Ter)

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