Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001433534 | SCV001636325 | likely benign | Developmental and epileptic encephalopathy, 1; Autosomal dominant nonsyndromic hearing loss 65; Caused by mutation in the TBC1 domain family, member 24 | 2022-04-16 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000863695 | SCV001834302 | likely benign | not provided | 2020-07-02 | criteria provided, single submitter | clinical testing |