Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV003765268 | SCV000252935 | likely benign | Familial adenomatous polyposis 1 | 2023-10-09 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000604328 | SCV000715940 | likely benign | not specified | 2017-02-10 | 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. |
Quest Diagnostics Nichols Institute San Juan Capistrano | RCV000758741 | SCV000887551 | likely benign | not provided | 2018-05-02 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV001026135 | SCV001188456 | likely benign | Hereditary cancer-predisposing syndrome | 2017-09-30 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. |