Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ce |
RCV000995163 | SCV001149198 | likely benign | not provided | 2024-01-01 | criteria provided, single submitter | clinical testing | FOXG1: BP4, BP7 |
Labcorp Genetics |
RCV001394821 | SCV001596511 | likely benign | Rett syndrome, congenital variant | 2022-11-01 | criteria provided, single submitter | clinical testing |