Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV003744619 | SCV000768363 | likely benign | Familial adenomatous polyposis 1 | 2023-04-07 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV001191941 | SCV001359882 | likely benign | Hereditary cancer-predisposing syndrome | 2019-09-19 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004004084 | SCV004822626 | likely benign | Classic or attenuated familial adenomatous polyposis | 2023-02-24 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV004025703 | SCV004932133 | likely benign | Familial adenomatous polyposis 1 | 2024-02-23 | criteria provided, single submitter | clinical testing | This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing. |