Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000442284 | SCV000531439 | likely benign | not specified | 2016-09-08 | 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. |
Ce |
RCV000994537 | SCV001148133 | uncertain significance | not provided | 2016-10-01 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001499051 | SCV001703808 | likely benign | Early infantile epileptic encephalopathy with suppression bursts | 2023-12-19 | criteria provided, single submitter | clinical testing |