Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV002068743 | SCV002335779 | likely benign | Duchenne muscular dystrophy | 2023-03-17 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002346207 | SCV002651016 | likely benign | Cardiovascular phenotype | 2021-10-06 | 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. |