List of variants reported as likely benign for autosomal recessive juvenile Parkinson disease 2

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Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_004562.3(PRKN):c.500G>A (p.Ser167Asn)	rs1801474	0.05277
NM_004562.3(PRKN):c.1180G>A (p.Asp394Asn)	rs1801334	0.02570
NM_004562.3(PRKN):c.*94A>G	rs62637702	0.02462
NM_004562.3(PRKN):c.*1695G>A	rs77283740	0.01596
NM_004562.3(PRKN):c.783A>G (p.Leu261=)	rs9456711	0.01329
NM_004562.3(PRKN):c.*1252C>T	rs77926621	0.01179
NM_004562.3(PRKN):c.*1462C>A	rs11961229	0.00787
NM_004562.3(PRKN):c.*1407C>T	rs11961237	0.00780
NM_004562.3(PRKN):c.*2187C>T	rs116309008	0.00713
NM_004562.3(PRKN):c.*2354C>T	rs191130749	0.00685
NM_004562.3(PRKN):c.*2217G>A	rs138660139	0.00678
NM_004562.3(PRKN):c.*1909G>A	rs148426411	0.00674
NM_004562.3(PRKN):c.-30T>C	rs200065081	0.00671
NM_004562.3(PRKN):c.136G>A (p.Ala46Thr)	rs75860381	0.00621
NM_004562.3(PRKN):c.458C>G (p.Pro153Arg)	rs55654276	0.00452
NM_004562.3(PRKN):c.101A>G (p.Gln34Arg)	rs148851677	0.00303
NM_004562.3(PRKN):c.*15C>A	rs35125035	0.00163
NM_004562.3(PRKN):c.919C>T (p.Leu307=)	rs138920699	0.00076
NM_004562.3(PRKN):c.837C>T (p.His279=)	rs149433924	0.00014
NM_004562.3(PRKN):c.1000C>T (p.Arg334Cys)	rs199657839	0.00004
NM_004562.3(PRKN):c.219G>A (p.Pro73=)	rs139083077	0.00004
NM_004562.3(PRKN):c.276G>A (p.Ala92=)	rs200256562	0.00004
NM_004562.3(PRKN):c.814C>A (p.Leu272Ile)	rs141366047	0.00004
NM_004562.3(PRKN):c.245C>A (p.Ala82Glu)	rs55774500

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