Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002542229 | SCV001667538 | likely benign | Familial adenomatous polyposis 1 | 2018-09-12 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV002542229 | SCV005085483 | benign | Familial adenomatous polyposis 1 | 2024-04-08 | 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. |