List of variants in gene PRKN reported as likely benign by Illumina Laboratory Services, Illumina

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: 14

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HGVS	dbSNP	gnomAD frequency
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.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.814C>A (p.Leu272Ile)	rs141366047	0.00004

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