ClinVar Miner

Submissions for variant NM_020247.5(COQ8A):c.1706C>A (p.Ala569Asp)

gnomAD frequency: 0.00001  dbSNP: rs765235707
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
Athena Diagnostics RCV000710477 SCV000840706 uncertain significance not provided 2018-04-30 criteria provided, single submitter clinical testing
Mendelics RCV002249431 SCV002519430 pathogenic Autosomal recessive ataxia due to ubiquinone deficiency 2022-05-04 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.