Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000775145 | SCV000909273 | likely benign | Hereditary cancer-predisposing syndrome | 2017-12-19 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV001459035 | SCV001662868 | likely benign | Hereditary breast ovarian cancer syndrome | 2023-10-30 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV000112288 | SCV004830873 | likely benign | Breast-ovarian cancer, familial, susceptibility to, 1 | 2023-12-01 | criteria provided, single submitter | clinical testing | |
Breast Cancer Information Core |
RCV000112288 | SCV000145020 | uncertain significance | Breast-ovarian cancer, familial, susceptibility to, 1 | 2003-12-23 | no assertion criteria provided | clinical testing |