Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000461332 | SCV000561812 | likely benign | Lethal congenital glycogen storage disease of heart | 2019-05-02 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002455891 | SCV002617866 | likely benign | Cardiovascular phenotype | 2018-09-14 | 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. |