Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003776658 | SCV002956421 | likely benign | Familial adenomatous polyposis 1 | 2022-02-18 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV003776658 | SCV004932355 | benign | Familial adenomatous polyposis 1 | 2024-03-07 | 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. |