Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Centre for Mendelian Genomics, |
RCV000626522 | SCV000747223 | uncertain significance | Coarctation of aorta; Tall stature; Specific learning disability | 2017-01-01 | criteria provided, single submitter | clinical testing |