Variant: rs1085307938 

    present in Gene: CLCN2
    present in Chromosome: 3
    Position on Chromosome: 184359124
    Alleles of this Variant: C/T

rs1085307938 in CLCN2 gene and Hyperaldosteronism, Familial, Type II PMID 29403012 2018 A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism.