Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000603509 | SCV000726528 | likely benign | not specified | 2018-01-14 | 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 | RCV002064258 | SCV002441733 | likely benign | Adams-Oliver syndrome 5 | 2024-01-11 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV002064258 | SCV002554929 | likely benign | Adams-Oliver syndrome 5 | 2022-03-15 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV002270839 | SCV002554930 | likely benign | Aortic valve disease 1 | 2022-03-15 | criteria provided, single submitter | clinical testing |