Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000838146 | SCV000980010 | benign | not provided | 2018-06-14 | 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. |
Genome- |
RCV001785736 | SCV002026859 | benign | Adams-Oliver syndrome 5 | 2021-09-05 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001785735 | SCV002026860 | benign | Aortic valve disease 1 | 2021-09-05 | criteria provided, single submitter | clinical testing |