Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center for Genomic Medicine, |
RCV003989042 | SCV004805537 | likely benign | Holoprosencephaly 5 | 2024-03-25 | criteria provided, single submitter | research |