ClinVar Miner

Submissions for variant NM_000506.5(F2):c.1298+19G>A

gnomAD frequency: 0.00003  dbSNP: rs753976233
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
ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology RCV002222130 SCV002499580 uncertain significance Thrombophilia due to thrombin defect criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003626694 SCV004383512 likely benign Congenital prothrombin deficiency 2023-12-05 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.