Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ce |
RCV001093032 | SCV001249824 | likely pathogenic | not provided | 2020-01-01 | criteria provided, single submitter | clinical testing | |
Pars Genome Lab | RCV003444152 | SCV004171106 | pathogenic | Rett syndrome, congenital variant | criteria provided, single submitter | clinical testing |