Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Illumina Laboratory Services, |
RCV000372894 | SCV000483895 | likely benign | Lynch syndrome | 2016-06-14 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001540929 | SCV001758867 | benign | not provided | 2018-06-23 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 24710284) |