Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV004565192 | SCV002345640 | likely benign | Familial adenomatous polyposis 1 | 2021-01-18 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV004565192 | SCV005084261 | benign | Familial adenomatous polyposis 1 | 2024-04-03 | 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. |