Total submissions: 6
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000629107 | SCV000750020 | likely benign | Hypertrophic cardiomyopathy | 2024-07-11 | criteria provided, single submitter | clinical testing | |
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, |
RCV001256694 | SCV001433093 | likely benign | not specified | 2019-09-12 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001672900 | SCV001883528 | benign | not provided | 2015-03-03 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV001805231 | SCV002052544 | likely benign | Cardiomyopathy | 2021-05-04 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV001805231 | SCV004823944 | likely benign | Cardiomyopathy | 2023-11-02 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV004025350 | SCV004943785 | likely benign | Cardiovascular phenotype | 2020-07-21 | 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. |