Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000197603 | SCV000253113 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2024-01-16 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV000565951 | SCV000670116 | likely benign | Hereditary cancer-predisposing syndrome | 2017-08-31 | 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. |
Color Diagnostics, |
RCV000565951 | SCV000690410 | likely benign | Hereditary cancer-predisposing syndrome | 2017-10-28 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV003996957 | SCV004826677 | likely benign | Lynch syndrome | 2023-03-23 | criteria provided, single submitter | clinical testing |