List of variants in gene PRKN reported as benign by Invitae

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_004562.3(PRKN):c.871+90882A>T	rs969759	0.56947
NM_004562.3(PRKN):c.8-3854C>G	rs12193297	0.45732
NM_004562.3(PRKN):c.172-19T>A	rs771310483	0.07440
NM_004562.3(PRKN):c.111G>A (p.Pro37=)	rs77795533	0.03342
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.574A>C (p.Met192Leu)	rs9456735	0.01850
NM_004562.3(PRKN):c.172-17dup	rs776880599	0.01724
NM_004562.3(PRKN):c.783A>G (p.Leu261=)	rs9456711	0.01329
NM_004562.3(PRKN):c.957T>C (p.Gly319=)	rs144340740	0.01025
NM_004562.3(PRKN):c.136G>A (p.Ala46Thr)	rs75860381	0.00621
NM_004562.3(PRKN):c.714C>T (p.Cys238=)	rs114974496	0.00357
NM_004562.3(PRKN):c.101A>G (p.Gln34Arg)	rs148851677	0.00303
NM_004562.3(PRKN):c.48G>A (p.Glu16=)	rs143477190	0.00270
NM_004562.3(PRKN):c.1204C>T (p.Arg402Cys)	rs55830907	0.00191
NM_004562.3(PRKN):c.535-9T>A	rs201039350	0.00038
NM_004562.3(PRKN):c.1083+18C>T	rs777171316	0.00006
NM_004562.3(PRKN):c.1000C>T (p.Arg334Cys)	rs199657839	0.00004
NM_004562.3(PRKN):c.1017G>A (p.Ala339=)	rs546676036	0.00003
NM_004562.3(PRKN):c.816C>T (p.Leu272=)	rs143902760	0.00002
NM_004562.3(PRKN):c.1138G>A (p.Val380Ile)
NM_004562.3(PRKN):c.1138G>C (p.Val380Leu)	rs1801582
NM_004562.3(PRKN):c.1138G>T (p.Val380Leu)	rs1801582
NM_004562.3(PRKN):c.171+20del	rs529531705
NM_004562.3(PRKN):c.172-18del
NM_004562.3(PRKN):c.172-28_172-18del	rs751742289
NM_004562.3(PRKN):c.245C>A (p.Ala82Glu)	rs55774500
NM_004562.3(PRKN):c.934-20_934-16del	rs545744886

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