Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000776852 | SCV000912516 | likely benign | Hereditary cancer-predisposing syndrome | 2017-11-20 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV004027300 | SCV002404366 | likely benign | Familial adenomatous polyposis 1 | 2023-11-17 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV004027300 | SCV004933399 | benign | Familial adenomatous polyposis 1 | 2024-02-22 | criteria provided, single submitter | clinical testing | This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing. |