Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Centre for Mendelian Genomics, |
RCV000626493 | SCV000747194 | uncertain significance | Alopecia areata; Stereotypic movement disorder; Developmental regression; Incomprehensible speech; Alopecia | 2017-01-01 | criteria provided, single submitter | clinical testing |