Variant: rs12979860 

    present in Gene: IFNL4
    present in Chromosome: 19
    Position on Chromosome: 39248147
    Alleles of this Variant: C/T

rs12979860 in IFNL4 gene and Hepatitis C, Chronic PMID 23420232 2013 Genome-wide association study of spontaneous resolution of hepatitis C virus infection: data from multiple cohorts.

PMID 19684573 2009 Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance.