Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000772370 | SCV000905548 | uncertain significance | Hereditary cancer-predisposing syndrome | 2018-09-30 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002536627 | SCV003343204 | likely benign | Familial cancer of breast | 2023-11-11 | criteria provided, single submitter | clinical testing |