Variant: rs142630661 

    present in Gene: FAM86C1;ALG1L9P
    present in Chromosome: 11
    Position on Chromosome: 71794579
    Alleles of this Variant: C/G

rs142630661 in FAM86C1;ALG1L9P 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.