Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001180124 | SCV001344990 | likely benign | Hereditary cancer-predisposing syndrome | 2016-04-27 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001875972 | SCV002176917 | likely benign | Peutz-Jeghers syndrome | 2024-01-10 | criteria provided, single submitter | clinical testing |