Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000777533 | SCV000913396 | likely benign | Hereditary cancer-predisposing syndrome | 2018-02-12 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002535621 | SCV003232598 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2022-09-05 | criteria provided, single submitter | clinical testing |