Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000182682 | SCV000235061 | uncertain significance | not provided | 2023-09-22 | criteria provided, single submitter | clinical testing | Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge |
Invitae | RCV003765126 | SCV004678084 | likely benign | Catecholaminergic polymorphic ventricular tachycardia 1 | 2023-02-01 | criteria provided, single submitter | clinical testing |