Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000584312 | SCV000686837 | likely benign | Hereditary cancer-predisposing syndrome | 2016-08-05 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003767280 | SCV002419892 | benign | Familial adenomatous polyposis 1 | 2023-10-22 | criteria provided, single submitter | clinical testing |