ClinVar Miner

Submissions for variant NM_138413.4(HOGA1):c.212-21A>G (rs11817730)

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
Nilou-Genome Lab RCV000186461 SCV001754875 likely benign Primary hyperoxaluria, type III 2021-07-10 criteria provided, single submitter clinical testing
GeneDx RCV001682896 SCV001903832 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Clinical Biochemistry Laboratory,Health Services Laboratory RCV000186461 SCV000239819 uncertain significance Primary hyperoxaluria, type III 2014-11-27 no assertion criteria provided research

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.