Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001179883 | SCV001344683 | likely benign | Hereditary cancer-predisposing syndrome | 2018-11-12 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001442727 | SCV001645680 | likely benign | Familial adenomatous polyposis 2 | 2023-10-22 | criteria provided, single submitter | clinical testing |