Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genetic Diagnostic Laboratory, |
RCV000655932 | SCV000583529 | likely pathogenic | Holoprosencephaly 7 | 2017-07-09 | criteria provided, single submitter | clinical testing |