Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000620308 | SCV000737485 | likely benign | Cardiovascular phenotype | 2016-04-04 | 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. |
Invitae | RCV000871082 | SCV001012681 | likely benign | Brugada syndrome 8 | 2024-01-20 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001591381 | SCV001815049 | likely benign | not provided | 2020-10-09 | criteria provided, single submitter | clinical testing |