Variant: rs55797039 

    present in Gene: LOC105369626;SCNN1A
    present in Chromosome: 12
    Position on Chromosome: 6363586
    Alleles of this Variant: G/A;T

rs55797039 in LOC105369626;SCNN1A gene and Adverse effects, not elsewhere classified PMID 30420678 2019 Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records.