Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000775330 | SCV000909595 | likely benign | Hereditary cancer-predisposing syndrome | 2017-11-30 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV000775330 | SCV001184052 | likely benign | Hereditary cancer-predisposing syndrome | 2019-10-08 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: 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 | RCV003744646 | SCV002414006 | likely benign | Familial adenomatous polyposis 1 | 2023-12-27 | criteria provided, single submitter | clinical testing |