Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000434285 | SCV000523506 | likely benign | not specified | 2017-11-06 | 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 | RCV003535714 | SCV000768319 | likely benign | Familial adenomatous polyposis 1 | 2023-12-08 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV001186321 | SCV001352706 | likely benign | Hereditary cancer-predisposing syndrome | 2019-11-11 | criteria provided, single submitter | clinical testing |