Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001222230 | SCV001394323 | likely benign | Colorectal cancer, susceptibility to, 10 | 2022-06-20 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002322076 | SCV002608157 | likely benign | Hereditary cancer-predisposing syndrome | 2019-11-15 | 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. |