Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV003535632 | SCV000282790 | likely benign | Familial adenomatous polyposis 1 | 2023-08-16 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV001183556 | SCV001349335 | likely benign | Hereditary cancer-predisposing syndrome | 2017-03-28 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV001183556 | SCV002654704 | likely benign | Hereditary cancer-predisposing syndrome | 2018-07-06 | 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. |