ClinVar Miner

Submissions for variant NM_001451.3(FOXF1):c.*1175_*1176del

dbSNP: rs397854726
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
Illumina Laboratory Services, Illumina RCV000310628 SCV000399231 benign Alveolar capillary dysplasia with pulmonary venous misalignment 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001672528 SCV001884903 benign not provided 2021-05-27 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.