Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000567356 | SCV000662440 | likely benign | Hereditary cancer-predisposing syndrome | 2016-02-07 | 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. |
Invitae | RCV001347674 | SCV001541946 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2022-08-22 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV000567356 | SCV001736270 | likely benign | Hereditary cancer-predisposing syndrome | 2020-05-11 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004000870 | SCV004836298 | likely benign | Lynch syndrome | 2023-11-30 | criteria provided, single submitter | clinical testing |