Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000250034 | SCV000305867 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Gene |
RCV001640498 | SCV001861572 | benign | not provided | 2019-04-03 | criteria provided, single submitter | clinical testing | |
National Health Laboratory Service, |
RCV002225546 | SCV002505222 | benign | Hereditary breast ovarian cancer syndrome | 2022-04-19 | criteria provided, single submitter | clinical testing | |
KCCC/NGS Laboratory, |
RCV003316354 | SCV004017643 | benign | Fanconi anemia complementation group D2 | 2023-07-07 | criteria provided, single submitter | clinical testing |