Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000776821 | SCV000912477 | likely benign | Hereditary cancer-predisposing syndrome | 2017-11-17 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003653314 | SCV003468349 | likely benign | Familial adenomatous polyposis 1 | 2022-04-12 | criteria provided, single submitter | clinical testing |