ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.1101T>C (p.Asn367=)

gnomAD frequency: 0.01928  dbSNP: rs114523318
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000972692 SCV001120415 benign not provided 2025-01-30 criteria provided, single submitter clinical testing
GeneDx RCV000972692 SCV001845445 benign not provided 2019-12-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002505478 SCV002803388 likely benign Glomerulopathy with fibronectin deposits 2; Spondylometaphyseal dysplasia - Sutcliffe type 2021-10-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000972692 SCV005243912 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.