Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001185332 | SCV001351527 | likely benign | Hereditary cancer-predisposing syndrome | 2018-11-20 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003650632 | SCV001609469 | likely benign | Familial adenomatous polyposis 1 | 2019-11-30 | criteria provided, single submitter | clinical testing |