Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000409894 | SCV000490019 | likely benign | Fanconi anemia complementation group O | 2016-09-28 | criteria provided, single submitter | clinical testing | |
Counsyl | RCV000411529 | SCV000490020 | likely benign | Breast-ovarian cancer, familial, susceptibility to, 3 | 2016-09-28 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000441287 | SCV000531722 | likely benign | not specified | 2017-03-23 | 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, |
RCV000580220 | SCV000686396 | likely benign | Hereditary cancer-predisposing syndrome | 2017-04-13 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000409894 | SCV002461225 | likely benign | Fanconi anemia complementation group O | 2023-11-06 | criteria provided, single submitter | clinical testing |