Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000663102 | SCV000786213 | likely benign | Hereditary diffuse gastric adenocarcinoma | 2018-03-22 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV001187080 | SCV001353744 | likely benign | Hereditary cancer-predisposing syndrome | 2023-05-09 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV000663102 | SCV002398093 | likely benign | Hereditary diffuse gastric adenocarcinoma | 2023-11-24 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV000663102 | SCV004019574 | uncertain significance | Hereditary diffuse gastric adenocarcinoma | 2023-03-03 | criteria provided, single submitter | clinical testing | This variant is classified as a variant of uncertain significance as there is insufficient evidence to determine its impact on protein function and/or cancer risk. |