Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001713676 | SCV001945709 | benign | not provided | 2015-03-03 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001796701 | SCV002033419 | benign | Fanconi anemia complementation group O | 2021-11-07 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV001713676 | SCV005252836 | benign | not provided | criteria provided, single submitter | not provided | ||
Clinical Genetics Laboratory, |
RCV001682699 | SCV001905782 | benign | not specified | no assertion criteria provided | clinical testing | ||
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, |
RCV001682699 | SCV001955278 | benign | not specified | no assertion criteria provided | clinical testing |