Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000584227 | SCV000687080 | likely benign | Hereditary cancer-predisposing syndrome | 2017-03-03 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003744595 | SCV003241394 | likely benign | Familial adenomatous polyposis 1 | 2022-10-10 | criteria provided, single submitter | clinical testing |