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Table 2 Genome-wide significant variants from GWAS across IFNβ preparations

From: Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS

ADA Variant Chr. Pos. (bp) MA MAF (KI) MAF (TUM) OR/β (Disc.) p (Disc.) OR/β (Repl.) p(one-sided) (Repl.) OR/β (Pool.) p (Pool.)
nADA pres. rs9281971 6 32,596,722 (T)7 0.36 0.39 0.59OR 1.9 × 10− 11 0.44 OR 2.4 × 10−08 0.55 OR 2.3 × 10−17
nADA titer rs9271377 6 32,587,165 G 0.30 0.33 − 0.15β 4.0 × 10−11 − 0.17β 4.0 × 10−05 − 0.16β 1.5 × 10−14
nADA titer rs9281971 6 32,596,722 (T)7 0.36 0.39 − 0.14β 1.4 × 10−10 − 0.23β 4.6 × 10−09 −0.16β 2.5 × 10−17
bADA level rs9271377 6 32,587,165 G 0.30 0.33 − 0.23β 1.3 × 10−13 − 0.20β 8.5 × 10−05 −0.22β 1.2 × 10−16
bADA level rs9272071 6 32,599,487 C 0.32 0.38 − 0.21β 1.8 × 10−11 − 0.28β 2.0 × 10−08 −0.23β 4.5 × 10−18
  1. The top GWAS association signals that showed genome-wide significance in the discovery-stage analysis (α = 5 × 10−8) and replicated (α = 3 × 10−3) in the analysis across all three treatment preparations. For nADA presence, odds ratios are provided (marked by OR), and for quantitative ADA measures effect sizes (marked by β). For detailed association statistics, including conditional analyses, correlated HLA alleles, nearby genes, eQTL results, permutation p values, and preparation-specific association results, see Additional file 12. For locus-specific Manhattan plots of each locus, see Additional file 13. For forest plots of each association, including treatment preparation-specific effects, see Additional file 14. Abbreviations: Chr. chromosome; Pos. position in base pairs (build hg19); MA minor and effect allele; MAF minor allele frequency; KI Karolinska Institutet, Sweden; TUM Technical University of Munich, Germany; OR odds ratio; β effect size; Disc discovery; Repl. replication; Pool. pooled; pres. presence; (T)7 TTTTTTT