ClinVar Miner

Submissions for variant NM_005141.5(FGB):c.959-13_959-10del

dbSNP: rs140114081
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000248105 SCV000310853 benign not specified criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000374346 SCV000447771 benign Congenital afibrinogenemia 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001618436 SCV001842893 benign not provided 2021-06-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000374346 SCV001933429 benign Congenital afibrinogenemia 2021-08-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001618436 SCV003277794 benign not provided 2024-01-30 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.