Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Blueprint Genetics | RCV000208399 | SCV000263884 | uncertain significance | Primary familial hypertrophic cardiomyopathy | 2015-11-12 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001853301 | SCV002176489 | likely benign | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma; Arrhythmogenic right ventricular dysplasia 8 | 2022-12-06 | criteria provided, single submitter | clinical testing |