Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000632986 | SCV000754196 | likely benign | Retinoblastoma | 2023-12-30 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV001017485 | SCV001178570 | likely benign | Hereditary cancer-predisposing syndrome | 2019-04-05 | 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. |
All of Us Research Program, |
RCV000632986 | SCV004846311 | likely benign | Retinoblastoma | 2023-03-07 | criteria provided, single submitter | clinical testing |