Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002140114 | SCV002452182 | likely benign | Juvenile polyposis syndrome | 2023-09-12 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV002140114 | SCV005405538 | benign | Juvenile polyposis syndrome | 2024-07-30 | 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. |