Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000125311 | SCV000168756 | benign | not specified | 2014-02-14 | 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 | RCV000639606 | SCV000761185 | likely benign | Landau-Kleffner syndrome | 2023-06-04 | criteria provided, single submitter | clinical testing | |
Revvity Omics, |
RCV000639606 | SCV003817429 | uncertain significance | Landau-Kleffner syndrome | 2020-12-02 | criteria provided, single submitter | clinical testing |