Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001499179 | SCV001703936 | likely benign | Very long chain acyl-CoA dehydrogenase deficiency | 2024-01-02 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002405182 | SCV002708757 | likely benign | Inborn genetic diseases | 2022-07-06 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, 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. |