ClinVar Miner

Submissions for variant NM_198076.6(COX20):c.*18_*19insAAGAA

dbSNP: rs59190751
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001722091 SCV000564910 benign not provided 2017-11-30 criteria provided, single submitter clinical testing
GeneDx RCV000199734 SCV000251306 benign not specified 2013-09-05 flagged submission clinical testing The variant is found in MITONUC-MITOP panel(s).

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.