Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001189902 | SCV001357285 | likely benign | Hereditary cancer-predisposing syndrome | 2019-08-22 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002069093 | SCV002409891 | likely benign | PTEN hamartoma tumor syndrome | 2021-11-22 | criteria provided, single submitter | clinical testing |