Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome- |
RCV001537758 | SCV001754706 | benign | Amelogenesis imperfecta type 1A | 2021-07-08 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001537759 | SCV001754707 | benign | Junctional epidermolysis bullosa gravis of Herlitz | 2021-07-08 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001537783 | SCV001754740 | benign | Junctional epidermolysis bullosa, non-Herlitz type | 2021-07-08 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001713112 | SCV001939614 | benign | not provided | 2015-03-03 | criteria provided, single submitter | clinical testing |