Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000128096 | SCV000171687 | benign | not specified | 2013-01-08 | 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. |
Invitae | RCV000676974 | SCV001015793 | benign | not provided | 2024-01-18 | criteria provided, single submitter | clinical testing | |
Mayo Clinic Laboratories, |
RCV000676974 | SCV000802801 | uncertain significance | not provided | 2017-08-22 | no assertion criteria provided | clinical testing |