Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000583534 | SCV000687984 | likely benign | Hereditary cancer-predisposing syndrome | 2017-08-23 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000649788 | SCV000771622 | likely benign | BAP1-related tumor predisposition syndrome | 2024-01-19 | criteria provided, single submitter | clinical testing |