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
Download table as spreadsheet
HGVS dbSNP
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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.