Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000942063 | SCV001087976 | likely benign | Fanconi anemia complementation group O | 2023-12-08 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002363443 | SCV002665300 | likely benign | Hereditary cancer-predisposing syndrome | 2015-11-19 | 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. |