Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001180216 | SCV001345086 | likely benign | Hereditary cancer-predisposing syndrome | 2019-08-12 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003769961 | SCV004635718 | likely benign | PTEN hamartoma tumor syndrome | 2023-06-10 | criteria provided, single submitter | clinical testing |