Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV003651911 | SCV000562634 | likely benign | Familial adenomatous polyposis 1 | 2022-03-16 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV000571206 | SCV000667598 | likely benign | Hereditary cancer-predisposing syndrome | 2016-12-29 | 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. |
Color Diagnostics, |
RCV000571206 | SCV001352874 | likely benign | Hereditary cancer-predisposing syndrome | 2019-11-22 | criteria provided, single submitter | clinical testing |