| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal recessive pseudohypoaldosteronism type 1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal recessive pseudohypoaldosteronism type 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal recessive pseudohypoaldosteronism type 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | SCNN1A-related disorder | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Duplication (frameshift variant) | not provided | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Liddle syndrome 3 +4 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Bronchiectasis with or without elevated sweat chloride 2 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive pseudohypoaldosteronism type 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive pseudohypoaldosteronism type 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive pseudohypoaldosteronism type 1 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense 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) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Bronchiectasis with or without elevated sweat chloride 2 | |
| | | Microsatellite (inframe_deletion) | Neurodevelopmental delay | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Bronchiectasis with or without elevated sweat chloride 2 +3 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive pseudohypoaldosteronism type 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Bronchiectasis with or without elevated sweat chloride 2 | |
| | | Single nucleotide variant (nonsense) | Liddle syndrome 3 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive pseudohypoaldosteronism type 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 1 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive pseudohypoaldosteronism type 1 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Bronchiectasis with or without elevated sweat chloride 2 +1 more | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (splice acceptor variant) | SCNN1A-related disorder | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive pseudohypoaldosteronism type 1 +2 more | GPathogenic/Likely pathogenic |