ClinVar Miner

Submissions for variant NM_198578.3(LRRK2):c.149A>G (p.His50Arg) (rs2256408)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000518786 SCV000614033 benign not specified 2017-01-30 criteria provided, single submitter clinical testing
GeneReviews RCV000032408 SCV000056064 unknown Parkinson disease 8, autosomal dominant 2012-09-13 no assertion criteria provided curation Converted during submission to Uncertain significance.
Invitae RCV000032408 SCV000640124 benign Parkinson disease 8, autosomal dominant 2016-11-28 criteria provided, single submitter clinical testing

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.