Total submissions: 6
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001176119 | SCV001339967 | likely benign | Hereditary cancer-predisposing syndrome | 2023-09-04 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV001437751 | SCV001640615 | likely benign | Hereditary breast ovarian cancer syndrome | 2021-10-27 | criteria provided, single submitter | clinical testing | |
Sema4, |
RCV001176119 | SCV002538016 | uncertain significance | Hereditary cancer-predisposing syndrome | 2021-05-19 | criteria provided, single submitter | curation | |
All of Us Research Program, |
RCV000030986 | SCV004828697 | likely benign | Breast-ovarian cancer, familial, susceptibility to, 1 | 2023-09-17 | criteria provided, single submitter | clinical testing | |
Sharing Clinical Reports Project |
RCV000030986 | SCV000053578 | uncertain significance | Breast-ovarian cancer, familial, susceptibility to, 1 | 2011-06-01 | no assertion criteria provided | clinical testing | |
BRCAlab, |
RCV000030986 | SCV004244191 | uncertain significance | Breast-ovarian cancer, familial, susceptibility to, 1 | 2020-03-02 | no assertion criteria provided | clinical testing |