Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV003767040 | SCV000647708 | likely benign | Familial adenomatous polyposis 1 | 2024-01-28 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV000776367 | SCV000911778 | likely benign | Hereditary cancer-predisposing syndrome | 2016-05-03 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000840507 | SCV000982435 | likely benign | not provided | 2018-03-20 | 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. |