Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000124083 | SCV000167492 | benign | not specified | 2014-01-16 | 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 | RCV002055443 | SCV002401562 | benign | Long QT syndrome | 2024-01-20 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002477327 | SCV002797902 | benign | Timothy syndrome; Brugada syndrome 3; Long qt syndrome 8 | 2022-02-17 | criteria provided, single submitter | clinical testing |