ClinVar Miner

Submissions for variant NM_002225.5(IVD):c.1095T>C (p.Ala365=)

dbSNP: rs1595790601
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
Invitae RCV001451244 SCV001654871 likely benign Isovaleryl-CoA dehydrogenase deficiency 2020-09-23 criteria provided, single submitter clinical testing
GeneDx RCV000977514 SCV001845110 benign not provided 2015-03-03 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.