Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Centro Nacional de Genética Medica "Dr. |
RCV000856639 | SCV000966010 | pathogenic | Chromosome 17q11.2 deletion syndrome, 1.4Mb | 2019-01-01 | criteria provided, single submitter | clinical testing |