Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000468689 | SCV000555975 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2023-11-02 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV000579576 | SCV000684832 | likely benign | Hereditary cancer-predisposing syndrome | 2015-07-15 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000607621 | SCV000730907 | likely benign | not specified | 2017-03-17 | 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. |
All of Us Research Program, |
RCV004002032 | SCV004826034 | likely benign | Lynch syndrome | 2023-05-15 | criteria provided, single submitter | clinical testing |