Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, |
RCV000623891 | SCV000740356 | uncertain significance | Primary familial hypertrophic cardiomyopathy | 2016-07-26 | criteria provided, single submitter | clinical testing |