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1.

rs12979860 [Homo sapiens]
    TGAACCAGGGAGCTCCCCGAAGGCG[C/T]GAACCAGGGTTGAATTGCACTCCGC
    Chromosome:
    19:39248147
    Gene:
    IFNL4 (GeneView)
    Functional Consequence:
    intron variant
    Clinical significance:
    drug-response
    Validated:
    by 1000G,by 2hit 2allele,by cluster,by frequency,by hapmap
    Global MAF:
    T=0.3558/1782
    HGVS:
    NC_000019.10:g.39248147C>T, NC_000019.9:g.39738787C>T, NG_042193.1:g.1825G>A, NM_001276254.2:c.151-152G>A, NR_074079.1:n.429-152G>A

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