Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001697351 | SCV000716108 | likely benign | not provided | 2019-05-20 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002350453 | SCV002650638 | likely benign | Familial thoracic aortic aneurysm and aortic dissection | 2022-07-10 | 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 | RCV002529432 | SCV003513165 | benign | Adams-Oliver syndrome 5 | 2023-07-16 | criteria provided, single submitter | clinical testing |