Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000773715 | SCV000907414 | likely benign | Hereditary cancer-predisposing syndrome | 2018-08-14 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002234144 | SCV001708663 | likely benign | Familial adenomatous polyposis 1 | 2022-12-15 | criteria provided, single submitter | clinical testing |