ClinVar Miner

Submissions for variant NM_201550.4(LRRC10):c.453C>T (p.Ala151=)

gnomAD frequency: 0.00050  dbSNP: rs12229290
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 RCV000655489 SCV000777420 benign Dilated Cardiomyopathy, Dominant 2025-01-21 criteria provided, single submitter clinical testing
GeneDx RCV001775943 SCV002013188 likely benign not provided 2020-01-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001775943 SCV005216121 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.