Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000411567 | SCV000489144 | likely benign | Familial cancer of breast | 2016-08-25 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000418309 | SCV000512593 | benign | not specified | 2015-03-27 | 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, |
RCV000580155 | SCV000684544 | likely benign | Hereditary cancer-predisposing syndrome | 2017-01-03 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000411567 | SCV002446836 | likely benign | Familial cancer of breast | 2024-01-24 | criteria provided, single submitter | clinical testing |