Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000647232 | SCV000769021 | likely benign | Brugada syndrome 8 | 2023-12-15 | criteria provided, single submitter | clinical testing | |
Gene |
RCV002289942 | SCV002578689 | uncertain significance | not provided | 2022-04-05 | criteria provided, single submitter | clinical testing | Has not been previously published as pathogenic or benign to our knowledge; In silico analysis supports that this missense variant does not alter protein structure/function |