Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000583185 | SCV000686873 | likely benign | Hereditary cancer-predisposing syndrome | 2017-03-13 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003117350 | SCV003785580 | likely benign | Familial adenomatous polyposis 1 | 2022-07-07 | criteria provided, single submitter | clinical testing |