Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001183386 | SCV001349102 | likely benign | Familial thoracic aortic aneurysm and aortic dissection | 2019-07-26 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV001425121 | SCV001627735 | likely benign | Ehlers-Danlos syndrome, type 4 | 2021-11-19 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV001183386 | SCV004008127 | likely benign | Familial thoracic aortic aneurysm and aortic dissection | 2023-04-17 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, 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. |
All of Us Research Program, |
RCV001425121 | SCV004833813 | likely benign | Ehlers-Danlos syndrome, type 4 | 2023-12-14 | criteria provided, single submitter | clinical testing |