Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000616364 | SCV000731043 | likely benign | not specified | 2017-01-30 | 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 | RCV002528758 | SCV003490012 | likely benign | Familial cancer of breast; Fanconi anemia complementation group J | 2023-09-27 | criteria provided, single submitter | clinical testing |