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Of the 1.8 billion people worldwide infected with  Mycobacterium tuberculosis , 5–15% will develop active tuberculosis (TB). Approximately half will progress to active TB within the first 18 months after infection, presumably because they fail to mount an effective initial immune response. Here, in a genome-wide genetic study of early TB progression, we genotype 4002 active TB cases and their household contacts in Peru. We quantify genetic heritability (   \documentclass[12pt]{minimal} 				\usepackage{amsmath} 				\usepackage{wasysym}  				\usepackage{amsfonts}  				\usepackage{amssymb}  				\usepackage{amsbsy} 				\usepackage{mathrsfs} 				\usepackage{upgreek} 				\setlength{\oddsidemargin}{-69pt} 				\begin{document}$${\it{h}}_{\it{g}}^2$$\end{document}h    g    2) of early TB progression to be 21.2% (standard error 0.08). This suggests TB progression has a strong genetic basis, and is comparable to traits with well-established genetic bases. We identify a novel association between early TB progression and variants located in a putative enhancer region on chromosome 3q23 (rs73226617, OR = 1.18;  P  = 3.93 × 10 −8 ). With in silico and in vitro analyses we identify rs73226617 or rs148722713 as the likely functional variant and  ATP1B3  as a potential causal target gene with monocyte specific function.

Early progression to active tuberculosis is a highly heritable trait driven by 3q23 in Peruvians