Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000247071 | SCV000305872 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Gene |
RCV001640499 | SCV001858585 | benign | not provided | 2019-02-11 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001702382 | SCV001933130 | benign | Fanconi anemia complementation group D2 | 2021-08-10 | criteria provided, single submitter | clinical testing | |
National Health Laboratory Service, |
RCV002225549 | SCV002505235 | benign | Hereditary breast ovarian cancer syndrome | 2022-04-19 | criteria provided, single submitter | clinical testing | |
KCCC/NGS Laboratory, |
RCV001702382 | SCV004017634 | benign | Fanconi anemia complementation group D2 | 2023-07-07 | criteria provided, single submitter | clinical testing |