Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001548252 | SCV001768129 | likely benign | not provided | 2018-12-12 | criteria provided, single submitter | clinical testing | |
Al Jalila Children's Genomics Center, |
RCV001731898 | SCV001984036 | uncertain significance | Autosomal dominant nocturnal frontal lobe epilepsy 1 | 2020-09-20 | criteria provided, single submitter | clinical testing |