Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000864120 | SCV001004879 | likely benign | Alstrom syndrome | 2023-11-07 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002332780 | SCV002633663 | likely benign | Cardiovascular phenotype | 2019-06-29 | 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. |
Fulgent Genetics, |
RCV000864120 | SCV002795226 | likely benign | Alstrom syndrome | 2022-02-09 | criteria provided, single submitter | clinical testing |