Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000776883 | SCV000912549 | likely benign | Hereditary cancer-predisposing syndrome | 2017-11-23 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003768410 | SCV002485786 | likely benign | Familial adenomatous polyposis 1 | 2022-08-23 | criteria provided, single submitter | clinical testing |