Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000559925 | SCV000623365 | likely benign | Renal cell carcinoma | 2023-12-24 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV001017102 | SCV001178132 | likely benign | Hereditary cancer-predisposing syndrome | 2019-03-06 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. |
Gene |
RCV001584237 | SCV001814082 | likely benign | not provided | 2021-06-02 | criteria provided, single submitter | clinical testing |