Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001180435 | SCV001345368 | likely benign | Hereditary cancer-predisposing syndrome | 2019-04-22 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002560802 | SCV003460386 | likely benign | PTEN hamartoma tumor syndrome | 2021-11-26 | criteria provided, single submitter | clinical testing |