Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000772838 | SCV000906220 | likely benign | Hereditary cancer-predisposing syndrome | 2018-05-17 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000937891 | SCV001083685 | likely benign | Familial adenomatous polyposis 2 | 2023-12-18 | criteria provided, single submitter | clinical testing | |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV003387925 | SCV004099704 | likely benign | not specified | 2023-09-01 | criteria provided, single submitter | clinical testing |