ClinVar Miner

Submissions for variant NM_020166.5(MCCC1):c.1978-57G>T

gnomAD frequency: 0.93354  dbSNP: rs6786878
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
Pars Genome Lab RCV001527493 SCV001738525 benign 3-methylcrotonyl-CoA carboxylase 1 deficiency 2021-06-15 criteria provided, single submitter clinical testing
GeneDx RCV001673113 SCV001889720 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001673113 SCV005302548 benign not provided criteria provided, single submitter not provided

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.