Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001175760 | SCV001339472 | likely benign | Hereditary cancer-predisposing syndrome | 2019-05-21 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002068145 | SCV002428456 | likely benign | Li-Fraumeni syndrome | 2021-08-09 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001175760 | SCV002582274 | likely benign | Hereditary cancer-predisposing syndrome | 2022-06-18 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV002290610 | SCV002582936 | likely benign | Li-Fraumeni syndrome 1 | 2022-06-18 | criteria provided, single submitter | clinical testing |