Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000581428 | SCV000686820 | uncertain significance | Hereditary cancer-predisposing syndrome | 2019-02-23 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003537244 | SCV000768342 | likely benign | Familial adenomatous polyposis 1 | 2023-05-30 | criteria provided, single submitter | clinical testing |