Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001190852 | SCV001358445 | likely benign | Hereditary cancer-predisposing syndrome | 2016-03-21 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002560095 | SCV003451184 | likely benign | Familial adenomatous polyposis 2 | 2023-12-15 | criteria provided, single submitter | clinical testing |