Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000570861 | SCV000669599 | likely benign | Hereditary cancer-predisposing syndrome | 2017-02-28 | 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. |
Gene |
RCV000603851 | SCV000713923 | likely benign | not provided | 2018-04-03 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001423519 | SCV001626100 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2023-11-01 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004001030 | SCV004840924 | likely benign | Lynch syndrome | 2023-03-23 | criteria provided, single submitter | clinical testing |