Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001182142 | SCV001347496 | likely benign | Hereditary cancer-predisposing syndrome | 2019-03-12 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003650626 | SCV001631561 | likely benign | Familial adenomatous polyposis 1 | 2019-12-19 | criteria provided, single submitter | clinical testing |