ClinVar Miner

Submissions for variant NM_000722.4(CACNA2D1):c.355-14dup

dbSNP: rs142849270
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000200585 SCV000252728 benign Brugada syndrome 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001722101 SCV000730186 benign not provided 2018-06-11 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV000602132 SCV001920609 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000602132 SCV001952393 benign not specified no assertion criteria provided 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.