Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Rare Disease Genomics Group, |
RCV000488734 | SCV000576168 | pathogenic | Pulmonary hypertension, primary, 1 | no assertion criteria provided | literature only | ||
Wendy Chung Laboratory, |
RCV001823915 | SCV002073622 | not provided | Pulmonary arterial hypertension; Idiopathic and/or familial pulmonary arterial hypertension | no assertion provided | literature only |