| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant (5 prime UTR variant) | FOXF1-related disorder | |
| | | Single nucleotide variant (5 prime UTR variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Deletion | Idiopathic and/or familial pulmonary arterial hypertension | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (frameshift variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Microsatellite (inframe_insertion) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_deletion) | not provided | |
| | | Microsatellite (inframe_deletion) | not provided | |
| | | Microsatellite (inframe_deletion) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Insertion (inframe_insertion) | not provided | |
| | | Microsatellite (inframe_insertion) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Insertion (inframe_insertion) | not provided | |
| | | Deletion (inframe_deletion) | Alveolar capillary dysplasia with pulmonary venous misalignment +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (nonsense) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Duplication (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | FOXF1-related disorder | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | See cases | |
| | | Single nucleotide variant (nonsense) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (nonsense) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Microsatellite (frameshift variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Duplication (frameshift variant) | See cases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment +3 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (synonymous variant) | FOXF1-related disorder | |
| | | Single nucleotide variant (nonsense) | FOXF1-related disorder | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | not provided | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | FOXF1-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Pyloric stenosis, infantile hypertrophic, 5 | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | FOXF1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | FOXF1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (synonymous variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | VATER association | |
| | | Single nucleotide variant (nonsense) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Deletion (inframe_deletion) | not provided | |
| | | Microsatellite (frameshift variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | FOXF1-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |