Variant: rs137852706 

    present in Gene: SCNN1B
    present in Chromosome: 16
    Position on Chromosome: 23348708
    Alleles of this Variant: G/A

rs137852706 in SCNN1B gene and Pseudohypoaldosteronism, Type I, Autosomal Recessive PMID 8589714 1996 Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1.