Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000582716 | SCV000689389 | likely benign | Hereditary cancer-predisposing syndrome | 2016-06-08 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001493091 | SCV001697713 | likely benign | Familial cancer of breast; Fanconi anemia complementation group J | 2024-01-24 | criteria provided, single submitter | clinical testing |