Four cytokine receptor genes are located on Chr21q22. 11, encoding the α and β subunits of the interferon-α receptor (IFNAR1 and IFNAR2), the β subunit of the interleukin 10 receptor (IL10RB) and the second subunit of the interferon-γ receptor (IFNGR2). We previously reported that two variants in IFNAR1 were associated with susceptibility to malaria in Gambians. We now present an extensive fine-scale mapping of the associated region utilizing 45 additional genetic markers obtained from public databases and by sequencing a 44 kb region in and around the IFNAR1 gene in 24 Gambian children (12 cases/12 controls). Within the IFNAR1 gene, a newly studied C→ G single-nucleotide polymorphism (IFNAR1 272354c-g) at position− 576 relative to the transcription start was found to be more strongly associated with susceptibility to severe malaria. Association was observed in three populations: in Gambian (P= 0.002), Kenyan (P= 0.022) and Vietnamese (P= 0.005) case–control studies. When all three studies were combined, using the Mantel–Haenszel test, the presence of IFNAR1− 576G was associated with a substantially elevated risk of severe malaria (N= 2444, OR= 1.38, 95% CI: 1.17–1.64; P= 1.7× 10− 4). This study builds on previous work to further highlight the importance of the type-I interferon pathway in malaria susceptibility and illustrates the utility of typing SNPs within regions of high linkage disequilibrium in multiple populations to confirm initial positive associations.