Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000774397 | SCV000908099 | likely benign | Hereditary cancer-predisposing syndrome | 2018-10-16 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002534139 | SCV003458904 | likely benign | Familial cancer of breast; Fanconi anemia complementation group J | 2023-12-14 | criteria provided, single submitter | clinical testing |