Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002150930 | SCV002467245 | likely benign | Familial adenomatous polyposis 1 | 2022-04-18 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002500307 | SCV002806705 | likely benign | Desmoid disease, hereditary; Familial adenomatous polyposis 1; Hepatocellular carcinoma; Gastric cancer; Colorectal cancer; Gastric adenocarcinoma and proximal polyposis of the stomach | 2021-11-24 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV002150930 | SCV004931434 | likely benign | Familial adenomatous polyposis 1 | 2024-02-23 | criteria provided, single submitter | clinical testing | This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing. |