Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV002126110 | SCV002452966 | likely benign | not provided | 2022-09-27 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002494420 | SCV002796639 | likely benign | Acromelic frontonasal dysostosis; Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features | 2021-09-16 | criteria provided, single submitter | clinical testing |