Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genetic Services Laboratory, |
RCV000118164 | SCV000152515 | uncertain significance | not provided | 2013-12-23 | criteria provided, single submitter | clinical testing | |
Eurofins Ntd Llc |
RCV000118164 | SCV000230657 | uncertain significance | not provided | 2014-11-03 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV000515390 | SCV000611515 | uncertain significance | Epilepsy, familial temporal lobe, 1; Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 | 2017-05-23 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000652997 | SCV000774871 | benign | Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 | 2024-01-17 | criteria provided, single submitter | clinical testing | |
Athena Diagnostics Inc | RCV000118164 | SCV000843473 | uncertain significance | not provided | 2017-12-15 | criteria provided, single submitter | clinical testing |