ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.1530C>T (p.Ala510=)

gnomAD frequency: 0.01017  dbSNP: rs61263981
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000946674 SCV001092821 benign not provided 2024-01-22 criteria provided, single submitter clinical testing
GeneDx RCV000946674 SCV002038682 likely benign not provided 2021-02-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000946674 SCV005258353 likely benign not provided criteria provided, single submitter not provided

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.