Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000159784 | SCV000209806 | benign | Hereditary cancer-predisposing syndrome | 2014-01-13 | criteria provided, single submitter | clinical testing | The variant is found in HEREDICANCER,COLO-HEREDIC panel(s). |
Illumina Laboratory Services, |
RCV000382850 | SCV000405756 | likely benign | Oligodontia-cancer predisposition syndrome | 2016-06-14 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002498794 | SCV002811791 | likely benign | Oligodontia-cancer predisposition syndrome; Colorectal cancer | 2022-05-31 | criteria provided, single submitter | clinical testing |