Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000242940 | SCV000320131 | likely benign | Cardiovascular phenotype | 2015-09-04 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: 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. |
Color Diagnostics, |
RCV001190244 | SCV001357694 | likely benign | Cardiomyopathy | 2019-09-09 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003525893 | SCV004369199 | likely benign | Catecholaminergic polymorphic ventricular tachycardia 1 | 2023-12-28 | criteria provided, single submitter | clinical testing |