Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000649824 | SCV000771658 | likely benign | BAP1-related tumor predisposition syndrome | 2023-07-07 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV001182213 | SCV001347572 | likely benign | Hereditary cancer-predisposing syndrome | 2019-05-07 | criteria provided, single submitter | clinical testing |