Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000611087 | SCV000720003 | likely benign | not specified | 2017-06-02 | 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. |
Labcorp Genetics |
RCV003767534 | SCV004579172 | likely benign | Intellectual disability, autosomal dominant 6; Developmental and epileptic encephalopathy, 27 | 2023-08-10 | criteria provided, single submitter | clinical testing |