Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002076795 | SCV002321223 | likely benign | Aortic aneurysm, familial thoracic 4 | 2021-03-07 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002407335 | SCV002720523 | likely benign | Familial thoracic aortic aneurysm and aortic dissection | 2020-03-13 | 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. |
Fulgent Genetics, |
RCV002479844 | SCV002802784 | likely benign | Aortic aneurysm, familial thoracic 4; Visceral myopathy 2; Megacystis-microcolon-intestinal hypoperistalsis syndrome 2 | 2021-10-01 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV002407335 | SCV005430654 | likely benign | Familial thoracic aortic aneurysm and aortic dissection | 2024-07-29 | criteria provided, single submitter | clinical testing |