Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001184663 | SCV001350699 | likely benign | Hereditary cancer-predisposing syndrome | 2019-10-31 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001481894 | SCV001686252 | likely benign | Hereditary breast ovarian cancer syndrome | 2023-05-26 | criteria provided, single submitter | clinical testing |