Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV001011644 | SCV001171990 | likely benign | Hereditary cancer-predisposing syndrome | 2019-09-20 | 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. |
Color Diagnostics, |
RCV001011644 | SCV001358037 | likely benign | Hereditary cancer-predisposing syndrome | 2019-01-02 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001428492 | SCV001631192 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2022-02-20 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004004501 | SCV004828030 | likely benign | Lynch syndrome | 2023-10-06 | criteria provided, single submitter | clinical testing |