Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001300053 | SCV001489176 | likely benign | Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 | 2023-09-03 | criteria provided, single submitter | clinical testing | |
Revvity Omics, |
RCV003485704 | SCV004236575 | uncertain significance | Norman-Roberts syndrome | 2023-01-30 | criteria provided, single submitter | clinical testing |