Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV002315103 | SCV000739456 | likely benign | Familial thoracic aortic aneurysm and aortic dissection | 2016-11-29 | 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 | RCV001455976 | SCV001659749 | likely benign | Adams-Oliver syndrome 5 | 2023-05-22 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001570101 | SCV001794316 | likely benign | not provided | 2018-10-23 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001455976 | SCV002555131 | likely benign | Adams-Oliver syndrome 5 | 2022-03-15 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV002270899 | SCV002555133 | likely benign | Aortic valve disease 1 | 2022-03-15 | criteria provided, single submitter | clinical testing |