Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001654756 | SCV001869141 | benign | not provided | 2018-08-14 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001776267 | SCV002014060 | benign | Weill-Marchesani syndrome 3 | 2021-09-05 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001776266 | SCV002014061 | benign | Microspherophakia | 2021-09-05 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV001654756 | SCV005292274 | benign | not provided | criteria provided, single submitter | not provided |