Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001176140 | SCV001340019 | uncertain significance | Hereditary cancer-predisposing syndrome | 2018-11-02 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001478697 | SCV001682972 | likely benign | Peutz-Jeghers syndrome | 2023-06-07 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001478697 | SCV002057289 | likely benign | Peutz-Jeghers syndrome | 2021-07-15 | criteria provided, single submitter | clinical testing | |
Sema4, |
RCV001176140 | SCV002526953 | uncertain significance | Hereditary cancer-predisposing syndrome | 2021-04-20 | criteria provided, single submitter | curation |