ClinVar Miner

List of variants in gene PRKN reported as benign for Parkinson disease

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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NM_004562.3(PRKN):c.101A>G (p.Gln34Arg) rs148851677
NM_004562.3(PRKN):c.1096C>T (p.Arg366Trp) rs56092260
NM_004562.3(PRKN):c.111G>A (p.Pro37=) rs77795533
NM_004562.3(PRKN):c.1138G>C (p.Val380Leu) rs1801582
NM_004562.3(PRKN):c.1180G>A (p.Asp394Asn) rs1801334
NM_004562.3(PRKN):c.1204C>T (p.Arg402Cys) rs55830907
NM_004562.3(PRKN):c.136G>A (p.Ala46Thr) rs75860381
NM_004562.3(PRKN):c.245C>A (p.Ala82Glu) rs55774500
NM_004562.3(PRKN):c.458C>G (p.Pro153Arg) rs55654276
NM_004562.3(PRKN):c.500G>A (p.Ser167Asn) rs1801474
NM_004562.3(PRKN):c.574A>C (p.Met192Leu) rs9456735
NM_004562.3(PRKN):c.783A>G (p.Leu261=) rs9456711
NM_004562.3(PRKN):c.816C>T (p.Leu272=) rs143902760
NM_004562.3(PRKN):c.957T>C (p.Gly319=) rs144340740

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