Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000431418 | SCV000512589 | likely benign | not specified | 2015-11-23 | 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, |
RCV000580028 | SCV000684678 | likely benign | Hereditary cancer-predisposing syndrome | 2016-05-10 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002058888 | SCV002444372 | likely benign | Familial cancer of breast | 2024-01-28 | criteria provided, single submitter | clinical testing |