Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Rare Disease Genomics Group, |
RCV000488807 | SCV000576137 | pathogenic | Pulmonary hypertension, primary, 1 | no assertion criteria provided | literature only | ||
NIHR Bioresource Rare Diseases, |
RCV001003701 | SCV001162144 | pathogenic | Pulmonary arterial hypertension | no assertion criteria provided | research |