Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001182124 | SCV001347478 | likely benign | Hereditary cancer-predisposing syndrome | 2019-01-03 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV004564605 | SCV001625692 | likely benign | Familial adenomatous polyposis 1 | 2024-07-06 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV004564605 | SCV005082977 | benign | Familial adenomatous polyposis 1 | 2024-04-12 | 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. |