List of variants reported as pathogenic for Young-onset Parkinson disease by Fulgent Genetics, Fulgent Genetics

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_004562.3(PRKN):c.823C>T (p.Arg275Trp)	rs34424986	0.00226
NM_004562.3(PRKN):c.101_102del (p.Gln34fs)	rs55777503	0.00027
NM_004562.3(PRKN):c.719C>T (p.Thr240Met)	rs137853054	0.00016
GRCh37/hg19 4q22.1(chr4:90647764-90758128)
GRCh37/hg19 6q26(chr6:161969922-161990424)
GRCh37/hg19 6q26(chr6:162394320-162475157)
GRCh37/hg19 6q26(chr6:162622150-162622256)
GRCh37/hg19 6q26(chr6:162622150-162683772)
GRCh37/hg19 6q26(chr6:162864400-162864441)

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