ClinVar Miner

Submissions for variant NM_019616.4(F7):c.64+937C>T

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
ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology RCV002280994 SCV002569299 uncertain significance Congenital factor VII deficiency criteria provided, single submitter clinical testing
GeneDx RCV004591863 SCV005079643 uncertain significance not provided 2024-05-06 criteria provided, single submitter clinical testing In silico analysis indicates that this variant does not alter splicing; This variant is associated with the following publications: (PMID: 25582404)
Mayo Clinic Laboratories, Mayo Clinic RCV004591863 SCV005409654 uncertain significance not provided 2023-10-27 criteria provided, single submitter clinical testing BS1, BP4, BP7

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.