CLL/SLL susceptibility loci identified through genome-wide association studies and follow-up studies.

Notes: In regular font are original independent SNPs identified through GWAS. In italics font are SNPs in LD with the original GWAS SNPs. In bold font are independently validated SNPs used for eQTL analysis and risk alleles as called by the primary study. Nearest gene(s) map within ∼200 kb of each SNP.aOR, CI and P-trend quoted are per copy of risk allele (bold in column 5) from all data combined in the primary study. P-trend, significance of the association between each SNP and risk of CLL/SLL.bConditional analysis reportedly provided no evidence for an independent role compared to original SNP [4], [7], [12].cAcquired after fine-scale mapping.dSignificance obtained from combined analysis from refs [12] and [8].Abbreviations: LD, Linkage disequilibrium; OR, odds ratio; CLL/SLL, chronic lymphocytic leukemia/small lymphocytic lymphoma; CI, confidence interval.