Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Mendelics | RCV000986657 | SCV001135712 | benign | Lynch syndrome 1 | 2019-05-28 | criteria provided, single submitter | clinical testing | |
Institute of Human Genetics, |
RCV001262883 | SCV001440918 | likely benign | Breast carcinoma | 2019-01-01 | criteria provided, single submitter | clinical testing | |
Sema4, |
RCV002255600 | SCV002526767 | benign | Hereditary cancer-predisposing syndrome | 2020-12-12 | criteria provided, single submitter | curation | |
Institute for Biomarker Research, |
RCV002255600 | SCV004014923 | likely benign | Hereditary cancer-predisposing syndrome | 2023-03-09 | criteria provided, single submitter | clinical testing | |
Center for Genomic Medicine, |
RCV003493765 | SCV004243549 | likely benign | not specified | 2024-02-06 | criteria provided, single submitter | clinical testing |