Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000600852 | SCV000723442 | likely benign | not provided | 2019-02-08 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 21982064, 23810759) |
Labcorp Genetics |
RCV001472564 | SCV001676699 | likely benign | Rett syndrome, congenital variant | 2022-09-01 | criteria provided, single submitter | clinical testing |