“…In CLL, genetic factors or polymorphisms involved in the overexpression of CCR7 remain uncovered but one singlenucleotide polymorphism (SNP) in the CCR7 gene was strongly associated with the risk of acquiring CLL. Out of 6 tested SNPs (including rs11574665, rs2023906, rs2290065, rs3136685, rs3136687, and rs588019) (49,50), the major G allele in the SNP rs3136687, which is located at the first intron and is in linkage disequilibrium with rs11574665, was associated with a higher risk towards CLL whereas the minor A allele resulted in a protective effect (49). The authors found no differences in CCR7 expression for such allelic variants.…”