Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000441046 | SCV000534530 | likely benign | not specified | 2016-12-06 | 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, |
RCV001184555 | SCV001350564 | likely benign | Cardiomyopathy | 2019-06-04 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004000561 | SCV004827467 | likely benign | Arrhythmogenic right ventricular cardiomyopathy | 2023-12-01 | criteria provided, single submitter | clinical testing |