| | | Single nucleotide variant (missense variant) | Bronchiectasis with or without elevated sweat chloride 3 | |
| | | Single nucleotide variant (missense variant) | Bronchiectasis with or without elevated sweat chloride 3 | |
| | | Single nucleotide variant (missense variant) | Bronchiectasis with or without elevated sweat chloride 3 +3 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive pseudohypoaldosteronism type 1 +3 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive pseudohypoaldosteronism type 1 +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive pseudohypoaldosteronism type 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Bronchiectasis with or without elevated sweat chloride 3 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (synonymous variant) | Bronchiectasis with or without elevated sweat chloride 3 | |
| | | Duplication (frameshift variant) | Autosomal recessive pseudohypoaldosteronism type 1 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive pseudohypoaldosteronism type 1 +3 more | |
| | | Single nucleotide variant (intron variant) | Bronchiectasis with or without elevated sweat chloride 3 +4 more | |
| | | Single nucleotide variant (synonymous variant) | Bronchiectasis with or without elevated sweat chloride 3 +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive pseudohypoaldosteronism type 1 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Liddle syndrome 2 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Liddle syndrome 2 +2 more | |
| | | Single nucleotide variant (missense variant) | Liddle syndrome 2 +3 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | Liddle syndrome 2 +4 more | |
| | | Single nucleotide variant (intron variant) | Liddle syndrome 2 +4 more | |
| | | Single nucleotide variant (intron variant) | Liddle syndrome 2 +4 more | |
| | | Single nucleotide variant (missense variant) | Liddle syndrome 2 +4 more | |
| | | Single nucleotide variant (missense variant) | SCNN1G-related condition +4 more | |