Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001465688 | SCV001669679 | likely benign | Developmental and epileptic encephalopathy, 1; Autosomal dominant nonsyndromic hearing loss 65; Caused by mutation in the TBC1 domain family, member 24 | 2023-06-19 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001550639 | SCV001770998 | likely benign | not provided | 2020-07-13 | criteria provided, single submitter | clinical testing |