Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000249082 | SCV000308586 | likely benign | not specified | criteria provided, single submitter | clinical testing | ||
Gene |
RCV000249082 | SCV000513010 | likely benign | not specified | 2017-02-14 | 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. |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV000249082 | SCV004029358 | benign | not specified | 2023-07-21 | criteria provided, single submitter | clinical testing |