Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000428322 | SCV000531097 | likely benign | not specified | 2017-09-19 | 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, |
RCV000580247 | SCV000681730 | likely benign | Hereditary cancer-predisposing syndrome | 2017-01-16 | criteria provided, single submitter | clinical testing | |
Counsyl | RCV000662543 | SCV000785123 | likely benign | Familial adenomatous polyposis 1 | 2017-05-01 | criteria provided, single submitter | clinical testing |