Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genetic Services Laboratory, |
RCV000145984 | SCV000193133 | likely benign | not specified | 2013-02-08 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000145984 | SCV000241021 | likely benign | not specified | 2012-05-14 | criteria provided, single submitter | clinical testing | The variant is found in EPILEPSY panel(s). |
Invitae | RCV000808453 | SCV000948562 | likely benign | Rett syndrome, congenital variant | 2024-01-24 | criteria provided, single submitter | clinical testing |