Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000583391 | SCV000686965 | likely benign | Hereditary cancer-predisposing syndrome | 2017-08-02 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003538357 | SCV001006923 | likely benign | Familial adenomatous polyposis 1 | 2023-12-06 | criteria provided, single submitter | clinical testing |