Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
EGL Genetic Diagnostics, |
RCV000173363 | SCV000224465 | likely benign | not specified | 2017-02-22 | criteria provided, single submitter | clinical testing | |
Genetic Services Laboratory, |
RCV000173363 | SCV000596752 | uncertain significance | not specified | 2015-12-31 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001080868 | SCV000656358 | likely benign | Norman-Roberts syndrome; Epilepsy, familial temporal lobe, 7 | 2019-12-31 | criteria provided, single submitter | clinical testing | |
Athena Diagnostics Inc | RCV000556641 | SCV001145265 | benign | not provided | 2018-11-23 | criteria provided, single submitter | clinical testing |