Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ce |
RCV000994977 | SCV001148824 | uncertain significance | not provided | 2019-04-01 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002409324 | SCV002715003 | likely benign | Inborn genetic diseases | 2022-08-08 | 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. |