Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001680126 | SCV001899782 | benign | not provided | 2021-05-17 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001776282 | SCV002014228 | benign | Myopathy, centronuclear, 6, with fiber-type disproportion | 2021-09-05 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001776281 | SCV002014229 | benign | Split-foot malformation-mesoaxial polydactyly syndrome | 2021-09-05 | criteria provided, single submitter | clinical testing |