Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000074766 | SCV000107977 | no known pathogenicity | Lynch syndrome | 2013-09-05 | reviewed by expert panel | research | MAF >1% |
ARUP Laboratories, |
RCV000756349 | SCV000884135 | benign | not specified | 2018-07-19 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001646996 | SCV001857635 | benign | not provided | 2015-03-03 | criteria provided, single submitter | clinical testing | |
Center for Genomic Medicine, |
RCV000756349 | SCV002552273 | benign | not specified | 2023-08-15 | criteria provided, single submitter | clinical testing | |
KCCC/NGS Laboratory, |
RCV003315588 | SCV004015987 | benign | Lynch syndrome 5 | 2023-07-07 | criteria provided, single submitter | clinical testing |