List of variants in gene PRKN reported as benign for autosomal recessive juvenile Parkinson disease 2

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_004562.3(PRKN):c.*2480C>A	rs68121389	0.37695
NM_004562.3(PRKN):c.*2021G>A	rs1122470	0.12415
NM_004562.3(PRKN):c.*652C>T	rs71653629	0.11674
NM_004562.3(PRKN):c.*1296A>G	rs3734464	0.08312
NM_004562.3(PRKN):c.*2492A>G	rs117341007	0.04051
NM_004562.3(PRKN):c.*320C>A	rs71653628	0.03819
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.*820A>T	rs74701717	0.02439
NM_004562.3(PRKN):c.574A>C (p.Met192Leu)	rs9456735	0.01850
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.1310C>T (p.Pro437Leu)	rs149953814	0.00223
NM_004562.3(PRKN):c.1096C>T (p.Arg366Trp)	rs56092260	0.00012
NM_004562.3(PRKN):c.1138G>C (p.Val380Leu)	rs1801582
NM_004562.3(PRKN):c.172-18del
NM_004562.3(PRKN):c.172-38dup	rs751742289

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