Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001182438 | SCV001347876 | likely benign | Hereditary cancer-predisposing syndrome | 2019-11-25 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001475216 | SCV001679406 | likely benign | Hereditary breast ovarian cancer syndrome | 2019-04-25 | criteria provided, single submitter | clinical testing |