Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000427029 | SCV000515585 | likely benign | not specified | 2016-07-28 | 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. |
Labcorp Genetics |
RCV000529385 | SCV000626885 | benign | Chuvash polycythemia; Von Hippel-Lindau syndrome | 2023-10-24 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV000567819 | SCV000675802 | likely benign | Hereditary cancer-predisposing syndrome | 2016-08-05 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, 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. |
Sema4, |
RCV000567819 | SCV002534148 | likely benign | Hereditary cancer-predisposing syndrome | 2022-01-01 | criteria provided, single submitter | curation |