Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001697349 | SCV000716034 | likely benign | not provided | 2021-02-23 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000866569 | SCV001007682 | benign | Heterotopia, periventricular, X-linked dominant; Melnick-Needles syndrome; Oto-palato-digital syndrome, type II; Frontometaphyseal dysplasia | 2023-12-31 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002341550 | SCV002637611 | likely benign | Familial thoracic aortic aneurysm and aortic dissection | 2017-04-07 | 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. |