Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Cancer Genomics Group, |
RCV001030723 | SCV001193691 | uncertain significance | Hereditary breast ovarian cancer syndrome | 2019-05-01 | criteria provided, single submitter | research | |
All of Us Research Program, |
RCV004004681 | SCV004826356 | uncertain significance | Lynch syndrome | 2023-05-31 | criteria provided, single submitter | clinical testing |