Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000074619 | SCV000107871 | no known pathogenicity | Lynch syndrome | 2013-09-05 | reviewed by expert panel | research | MAF >1% |
Illumina Laboratory Services, |
RCV000074619 | SCV000483934 | likely benign | Lynch syndrome | 2016-06-14 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001618241 | SCV001842689 | benign | not provided | 2018-06-23 | criteria provided, single submitter | clinical testing |