ClinVar Miner

List of variants reported as uncertain significance for Parkinson disease by Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine

Included ClinVar conditions (34):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
Download table as spreadsheet
NM_003285.3(TNR):c.1732C>T (p.Arg578Ter) rs869312899
NM_003285.3(TNR):c.1774A>G (p.Thr592Ala) rs140481433
NM_003285.3(TNR):c.463T>A (p.Cys155Ser) rs150331590
NM_003285.3(TNR):c.496A>G (p.Thr166Ala) rs147204644
NM_003285.3(TNR):c.538A>C (p.Asn180His) rs61731112
NM_005781.4(TNK2):c.1088T>C (p.Val363Ala) rs370013968
NM_005781.4(TNK2):c.1912G>A (p.Val638Met) rs201407161
NM_005781.4(TNK2):c.2930C>T (p.Ala977Val) rs571171423

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.