Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
UW Hindbrain Malformation Research Program, |
RCV001258006 | SCV001442539 | pathogenic | Familial aplasia of the vermis | 2020-05-26 | criteria provided, single submitter | research | |
University of Washington Center for Mendelian Genomics, |
RCV001258006 | SCV001434820 | likely pathogenic | Familial aplasia of the vermis | no assertion criteria provided | research |