Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000610675 | SCV000730073 | likely benign | not specified | 2018-01-02 | 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. |
ARUP Laboratories, |
RCV001523604 | SCV001473481 | likely benign | not provided | 2019-11-25 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV001523604 | SCV001733337 | benign | not provided | 2024-01-26 | criteria provided, single submitter | clinical testing |