Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome Medicine, |
RCV001027748 | SCV000998765 | uncertain significance | Intellectual disability, X-linked, syndromic 33 | 2019-09-23 | no assertion criteria provided | clinical testing | |
Yale Center for Mendelian Genomics, |
RCV001849456 | SCV002106727 | association | Heart, malformation of | 2020-06-13 | no assertion criteria provided | literature only |