Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000249498 | SCV000306067 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Gene |
RCV000830386 | SCV000972121 | benign | not provided | 2018-06-16 | 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. |
Genome- |
RCV001795436 | SCV002033009 | benign | Arrhythmogenic right ventricular dysplasia 2 | 2021-11-07 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001843022 | SCV002033010 | benign | Cardiac arrhythmia | 2021-11-07 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001795437 | SCV002033011 | benign | Catecholaminergic polymorphic ventricular tachycardia 1 | 2021-11-07 | criteria provided, single submitter | clinical testing |