ClinVar Miner

Submissions for variant NM_198578.4(LRRK2):c.825= (p.His275=)

gnomAD frequency: 0.99959  dbSNP: rs72546315
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000032518 SCV000056181 unknown Autosomal dominant Parkinson disease 8 2012-09-13 no assertion criteria provided curation Converted during submission to Uncertain significance.

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.