Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000457227 | SCV000723738 | likely benign | not provided | 2020-05-12 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002313220 | SCV000739471 | likely benign | Familial thoracic aortic aneurysm and aortic dissection | 2017-07-30 | 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. |
Invitae | RCV001467492 | SCV001671516 | likely benign | Adams-Oliver syndrome 5 | 2024-01-29 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001467492 | SCV002554298 | benign | Adams-Oliver syndrome 5 | 2022-03-15 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV002270540 | SCV002554299 | benign | Aortic valve disease 1 | 2022-03-15 | criteria provided, single submitter | clinical testing |