Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000248902 | SCV000305858 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Genome- |
RCV001701957 | SCV001933097 | benign | Fanconi anemia complementation group D2 | 2021-08-10 | criteria provided, single submitter | clinical testing | |
National Health Laboratory Service, |
RCV002225542 | SCV002505199 | benign | Hereditary breast ovarian cancer syndrome | 2022-04-19 | criteria provided, single submitter | clinical testing | |
KCCC/NGS Laboratory, |
RCV001701957 | SCV004017631 | benign | Fanconi anemia complementation group D2 | 2023-07-07 | criteria provided, single submitter | clinical testing |