Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000126841 | SCV000170370 | benign | not specified | 2013-09-17 | 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. |
Color Diagnostics, |
RCV000449453 | SCV000537462 | likely benign | Hereditary cancer-predisposing syndrome | 2015-07-29 | criteria provided, single submitter | clinical testing | |
ARUP Laboratories, |
RCV000126841 | SCV000604275 | benign | not specified | 2018-10-08 | criteria provided, single submitter | clinical testing | |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV000030263 | SCV000052930 | likely benign | Lynch syndrome | 2015-10-02 | no assertion criteria provided | clinical testing |