Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Mendelics | RCV000986788 | SCV001135917 | uncertain significance | Pheochromocytoma | 2019-05-28 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001214275 | SCV001385950 | likely benign | Hereditary pheochromocytoma-paraganglioma | 2023-08-18 | criteria provided, single submitter | clinical testing |