Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000245041 | SCV000305883 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Gene |
RCV001636755 | SCV001852423 | benign | not provided | 2019-02-11 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001701890 | SCV001933086 | benign | Fanconi anemia complementation group D2 | 2021-08-10 | criteria provided, single submitter | clinical testing | |
National Health Laboratory Service, |
RCV002225559 | SCV002505189 | benign | Hereditary breast ovarian cancer syndrome | 2022-04-19 | criteria provided, single submitter | clinical testing | |
KCCC/NGS Laboratory, |
RCV001701890 | SCV004017629 | benign | Fanconi anemia complementation group D2 | 2023-07-07 | criteria provided, single submitter | clinical testing |