Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000582704 | SCV000687285 | likely benign | Hereditary cancer-predisposing syndrome | 2017-10-31 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV004592790 | SCV005082082 | likely benign | Familial cancer of breast | 2024-04-24 | criteria provided, single submitter | clinical testing | This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing. |