Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001476635 | SCV001680847 | likely benign | Rett syndrome, congenital variant | 2019-10-10 | criteria provided, single submitter | clinical testing | |
Ce |
RCV002264342 | SCV002545167 | likely benign | not provided | 2022-05-01 | criteria provided, single submitter | clinical testing | FOXG1: BP4, BP7 |