Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000185875 | SCV000238827 | benign | not specified | 2014-06-09 | criteria provided, single submitter | clinical testing | This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. |
Invitae | RCV001084836 | SCV000631950 | benign | Multiple acyl-CoA dehydrogenase deficiency | 2024-02-01 | criteria provided, single submitter | clinical testing | |
ARUP Laboratories, |
RCV001084836 | SCV004562846 | benign | Multiple acyl-CoA dehydrogenase deficiency | 2023-09-07 | criteria provided, single submitter | clinical testing | |
Mayo Clinic Laboratories, |
RCV000676880 | SCV000802694 | benign | not provided | 2017-08-04 | no assertion criteria provided | clinical testing |