Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001516983 | SCV001725364 | benign | Heterotopia, periventricular, X-linked dominant; Melnick-Needles syndrome; Oto-palato-digital syndrome, type II; Frontometaphyseal dysplasia | 2023-07-29 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000875867 | SCV001803331 | likely benign | not provided | 2021-04-14 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002320048 | SCV002632619 | likely benign | Familial thoracic aortic aneurysm and aortic dissection | 2018-05-24 | 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. |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV003323752 | SCV004029211 | likely benign | not specified | 2023-07-29 | criteria provided, single submitter | clinical testing |