Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001525730 | SCV001735913 | likely benign | Hereditary cancer-predisposing syndrome | 2020-11-09 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002568105 | SCV003353407 | likely benign | Familial adenomatous polyposis 2 | 2022-05-06 | criteria provided, single submitter | clinical testing |