Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000609953 | SCV000727422 | likely benign | not specified | 2018-02-23 | 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 | RCV000951020 | SCV001097372 | likely benign | Isovaleryl-CoA dehydrogenase deficiency | 2023-04-03 | criteria provided, single submitter | clinical testing |