Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001707757 | SCV000718844 | likely benign | not provided | 2018-03-28 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000960732 | SCV001107746 | likely benign | Ehlers-Danlos syndrome, kyphoscoliotic type 1 | 2023-12-19 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002438569 | SCV002747200 | likely benign | Familial thoracic aortic aneurysm and aortic dissection | 2018-03-20 | 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. |