ClinVar Miner

Submissions for variant NM_182925.5(FLT4):c.3198C>T (p.Pro1066=)

gnomAD frequency: 0.24024  dbSNP: rs1130378
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 7
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000254508 SCV000316804 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001668615 SCV001883630 benign not provided 2018-11-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701925 SCV001933504 benign Congenital heart defects, multiple types, 7 2021-08-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701831 SCV001933505 benign Hereditary lymphedema type I 2021-08-10 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000254508 SCV001741652 benign not specified no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000254508 SCV001918855 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000254508 SCV001953997 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.