Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000871976 | SCV001013721 | likely benign | Intellectual disability, autosomal dominant 6; Developmental and epileptic encephalopathy, 27 | 2023-09-08 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV004705836 | SCV005213784 | likely benign | not provided | criteria provided, single submitter | not provided |