Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001088822 | SCV000642192 | likely benign | Familial focal epilepsy with variable foci | 2019-12-31 | criteria provided, single submitter | clinical testing | |
Genome Diagnostics Laboratory, |
RCV000545790 | SCV000743136 | likely benign | Epilepsy, familial focal, with variable foci 1 | 2015-09-24 | criteria provided, single submitter | clinical testing | |
DNA and Cytogenetics Diagnostics Unit, |
RCV000545790 | SCV000744146 | likely benign | Epilepsy, familial focal, with variable foci 1 | 2016-01-18 | criteria provided, single submitter | clinical testing |