Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000583061 | SCV000689266 | likely benign | Hereditary cancer-predisposing syndrome | 2016-12-13 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV002530792 | SCV003328589 | likely benign | Familial cancer of breast; Fanconi anemia complementation group J | 2022-10-16 | criteria provided, single submitter | clinical testing |