Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV002231702 | SCV000631592 | likely benign | Ehlers-Danlos syndrome, classic type, 1 | 2017-06-12 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002323936 | SCV002609743 | likely benign | Familial thoracic aortic aneurysm and aortic dissection | 2019-07-22 | 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. |