Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000226815 | SCV000288908 | likely benign | Brugada syndrome 8 | 2023-12-07 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001582784 | SCV001811403 | likely benign | not provided | 2020-11-11 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002321877 | SCV002609896 | likely benign | Cardiovascular phenotype | 2019-10-24 | 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. |