Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000442165 | SCV000527781 | likely benign | not specified | 2017-02-06 | criteria provided, single submitter | clinical testing | This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. |
Color Diagnostics, |
RCV000777597 | SCV000913462 | likely benign | Cardiomyopathy | 2018-06-11 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002521782 | SCV002495130 | benign | Catecholaminergic polymorphic ventricular tachycardia 1 | 2024-01-31 | criteria provided, single submitter | clinical testing | |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV000442165 | SCV002600654 | benign | not specified | 2022-10-22 | criteria provided, single submitter | clinical testing |