Gene entry
SCNN1G
sodium channel epithelial 1 subunit gamma
- Chromosome
- 16
- Cytoband
- 16p12.2
- Variants (rsID)
- 25
SCNN1G is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p12.2). Its official name is “sodium channel epithelial 1 subunit gamma”. The reference table lists 25 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs13306653Benignsingle nucleotide variantAutosomal recessive pseudohypoaldosteronism type 1|Liddle syndrome 2|Bronchiectasis with or without elevated sweat chloride 3
- rs5723Benignsingle nucleotide variantAutosomal recessive pseudohypoaldosteronism type 1|Liddle syndrome 2|Bronchiectasis with or without elevated sweat chloride 3
- rs5729Benignsingle nucleotide variantLiddle syndrome 2|Autosomal recessive pseudohypoaldosteronism type 1
- rs5736Benignsingle nucleotide variantBronchiectasis with or without elevated sweat chloride 3|Autosomal recessive pseudohypoaldosteronism type 1|Liddle syndrome 2
- rs5738Benignsingle nucleotide variantBronchiectasis with or without elevated sweat chloride 3|Liddle syndrome 2|Autosomal recessive pseudohypoaldosteronism type 1
- rs5740Benignsingle nucleotide variantAutosomal recessive pseudohypoaldosteronism type 1|Liddle syndrome 2|Bronchiectasis with or without elevated sweat chloride 3
- rs148985177Conflicting interpretationssingle nucleotide variantLiddle syndrome 2|Autosomal recessive pseudohypoaldosteronism type 1|Bronchiectasis with or without elevated sweat chloride 3
- rs72646501Conflicting interpretationssingle nucleotide variantAutosomal recessive pseudohypoaldosteronism type 1|Liddle syndrome 2
- rs72647541Conflicting interpretationssingle nucleotide variantAutosomal recessive pseudohypoaldosteronism type 1|Liddle syndrome 2
- rs754747376Uncertain significancesingle nucleotide variantAutosomal recessive pseudohypoaldosteronism type 1|Liddle syndrome 2
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.