Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000584556 | SCV000689708 | likely benign | Hereditary cancer-predisposing syndrome | 2017-09-12 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000608969 | SCV000732763 | likely benign | not specified | 2017-06-16 | 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 | RCV001405567 | SCV001607496 | likely benign | Familial cancer of breast | 2018-03-23 | criteria provided, single submitter | clinical testing |