ClinVar Miner

List of variants reported as uncertain significance for Parkinson disease by Neurogenetic Laboratory,Oslo University Hospital

Included ClinVar conditions (34):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
Download table as spreadsheet
NM_007262.5(PARK7):c.399G>C (p.Met133Ile) rs398124657
NM_018206.6(VPS35):c.1576C>T (p.Arg526Cys) rs398124658
NM_032409.3(PINK1):c.644C>T (p.Pro215Leu) rs371854396
NM_032409.3(PINK1):c.923T>A (p.Leu308Gln) rs398124659
NM_198578.4(LRRK2):c.2352C>A (p.Ser784Arg) rs398124660
NM_198578.4(LRRK2):c.7300A>G (p.Ile2434Val) rs398124661

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.