Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001176615 | SCV001340651 | likely benign | Hereditary cancer-predisposing syndrome | 2018-05-15 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002555461 | SCV003495324 | likely benign | PTEN hamartoma tumor syndrome | 2022-12-07 | criteria provided, single submitter | clinical testing |