Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Hudson |
RCV001353173 | SCV001548334 | uncertain significance | Autosomal dominant Opitz G/BBB syndrome | 2021-03-25 | criteria provided, single submitter | research | ACMG codes:PM2; PP3 |