Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genomic Research Center, |
RCV000714712 | SCV000845438 | likely pathogenic | Amelogenesis imperfecta type 1G | 2018-08-07 | criteria provided, single submitter | clinical testing |