Variant: rs1553853557 

    present in Gene: CLCN2;FAM131A
    present in Chromosome: 3
    Position on Chromosome: 184346710
    Alleles of this Variant: T/G

rs1553853557 in CLCN2;FAM131A gene and Hyperaldosteronism, Familial, Type II PMID 29403011 2018 CLCN2 chloride channel mutations in familial hyperaldosteronism type II.

PMID 29403012 2018 A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism.