Total submissions: 6
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000252212 | SCV000311366 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Gene |
RCV000252212 | SCV000520317 | benign | not specified | 2016-09-22 | 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. |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV000252212 | SCV001774662 | benign | not specified | 2021-07-08 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002518635 | SCV002405169 | benign | Catecholaminergic polymorphic ventricular tachycardia 1 | 2024-02-01 | criteria provided, single submitter | clinical testing | |
Clinical Genetics, |
RCV000252212 | SCV001925751 | benign | not specified | no assertion criteria provided | clinical testing | ||
Diagnostic Laboratory, |
RCV000252212 | SCV001963177 | benign | not specified | no assertion criteria provided | clinical testing |