ClinVar Miner

Submissions for variant NM_032578.4(MYPN):c.1600+21G>C

gnomAD frequency: 0.00739  dbSNP: rs41278498
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000625074 SCV000743686 benign Dilated cardiomyopathy 1KK 2014-10-09 criteria provided, single submitter clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000625074 SCV000745048 benign Dilated cardiomyopathy 1KK 2015-09-21 criteria provided, single submitter clinical testing
GeneDx RCV001591402 SCV001815449 likely benign not provided 2018-06-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001591402 SCV005228107 likely 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.