Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001584864 | SCV001813798 | likely benign | not provided | 2020-08-03 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV002070412 | SCV002347903 | likely benign | Renal cell carcinoma | 2023-11-05 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002414280 | SCV002715321 | likely benign | Hereditary cancer-predisposing syndrome | 2020-01-14 | 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. |