Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000420380 | SCV000513524 | likely benign | not provided | 2016-12-09 | 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. |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV001778958 | SCV002014826 | benign | not specified | 2021-10-09 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV002061429 | SCV002358566 | benign | RASopathy | 2024-01-21 | criteria provided, single submitter | clinical testing |