Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001183609 | SCV001349402 | likely benign | Hereditary cancer-predisposing syndrome | 2019-03-29 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003505169 | SCV004313651 | likely benign | Familial adenomatous polyposis 2 | 2023-11-13 | criteria provided, single submitter | clinical testing |