Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000431295 | SCV000520148 | likely benign | not specified | 2017-04-26 | 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 | RCV000545928 | SCV000625667 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2024-01-18 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV000580981 | SCV000686217 | likely benign | Hereditary cancer-predisposing syndrome | 2017-01-12 | criteria provided, single submitter | clinical testing |