Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000842374 | SCV000984390 | likely benign | not provided | 2018-04-27 | 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. |
CHEO Genetics Diagnostic Laboratory, |
RCV001798991 | SCV002042384 | uncertain significance | Cardiomyopathy | 2021-04-01 | criteria provided, single submitter | clinical testing | |
Revvity Omics, |
RCV000842374 | SCV003827928 | uncertain significance | not provided | 2020-03-31 | criteria provided, single submitter | clinical testing |