Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center of Genomic medicine, |
RCV000504482 | SCV000598133 | likely pathogenic | Marfan syndrome | 2014-12-15 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV000504482 | SCV004829528 | uncertain significance | Marfan syndrome | 2023-05-16 | criteria provided, single submitter | clinical testing |