Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000171022 | SCV000223586 | benign | not specified | 2017-05-10 | 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. |
Invitae | RCV001842512 | SCV000554077 | benign | Cardiac arrhythmia | 2024-01-30 | criteria provided, single submitter | clinical testing | |
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, |
RCV000845313 | SCV000987355 | likely benign | not provided | criteria provided, single submitter | clinical testing | ||
Diagnostic Laboratory, |
RCV000171022 | SCV001963210 | benign | not specified | no assertion criteria provided | clinical testing | ||
Clinical Genetics, |
RCV000171022 | SCV001978837 | benign | not specified | no assertion criteria provided | clinical testing |