Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000442902 | SCV000515458 | likely benign | not specified | 2016-01-18 | 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, |
RCV000582017 | SCV000689998 | likely benign | Hereditary cancer-predisposing syndrome | 2017-09-22 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000630354 | SCV000751310 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2023-07-08 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV000582017 | SCV001172679 | likely benign | Hereditary cancer-predisposing syndrome | 2017-11-27 | 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. |
All of Us Research Program, |
RCV003996007 | SCV004831746 | likely benign | Lynch syndrome | 2023-06-08 | criteria provided, single submitter | clinical testing |