ClinVar Miner

Submissions for variant NM_000527.5(LDLR):c.2277C>T (p.Leu759=)

gnomAD frequency: 0.00002  dbSNP: rs796145467
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 RCV001409846 SCV001611880 likely benign Familial hypercholesterolemia 2024-01-19 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004006917 SCV004843837 likely benign Hypercholesterolemia, familial, 1 2023-11-20 criteria provided, single submitter clinical testing
Ambry Genetics RCV005369874 SCV006019646 likely benign Cardiovascular phenotype 2025-01-28 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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.