Total submissions: 6
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000253247 | SCV000305882 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Genome- |
RCV001701889 | SCV001933075 | benign | Fanconi anemia complementation group D2 | 2021-08-10 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001709528 | SCV001937622 | benign | not provided | 2019-02-11 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002057415 | SCV002477029 | benign | Fanconi anemia | 2024-02-01 | criteria provided, single submitter | clinical testing | |
National Health Laboratory Service, |
RCV002225558 | SCV002505188 | benign | Hereditary breast ovarian cancer syndrome | 2022-04-19 | criteria provided, single submitter | clinical testing | |
KCCC/NGS Laboratory, |
RCV001701889 | SCV004017628 | benign | Fanconi anemia complementation group D2 | 2023-07-07 | criteria provided, single submitter | clinical testing |