Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000475629 | SCV000562733 | likely benign | Hereditary Paraganglioma-Pheochromocytoma Syndromes | 2019-12-31 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV000563732 | SCV000675041 | likely benign | Hereditary cancer-predisposing syndrome | 2015-03-09 | criteria provided, single submitter | clinical testing | |
Ce |
RCV001090317 | SCV001245793 | likely benign | not provided | 2019-10-01 | criteria provided, single submitter | clinical testing |