Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome- |
RCV001549241 | SCV001769359 | benign | Weill-Marchesani 4 syndrome, recessive | 2021-07-14 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001615301 | SCV001838772 | benign | not provided | 2018-09-04 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV001615301 | SCV005291420 | benign | not provided | criteria provided, single submitter | not provided |