Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Department of Medical Genetics, |
RCV000627677 | SCV001451969 | pathogenic | Microcephaly 21, primary, autosomal recessive | criteria provided, single submitter | research | ||
OMIM | RCV000627677 | SCV000748675 | pathogenic | Microcephaly 21, primary, autosomal recessive | 2023-09-12 | no assertion criteria provided | literature only |