Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000773388 | SCV000907082 | likely benign | Hereditary cancer-predisposing syndrome | 2018-06-18 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003153832 | SCV001661155 | likely benign | Familial adenomatous polyposis 1 | 2024-01-17 | criteria provided, single submitter | clinical testing |