Figure 1.
Regional plot of SNP associations with normal cytogenetic B-ALL. Regional plot showing association with normal cytogenetic B-ALL in a region of chromosome 14 (rs189434316). The x-axis is the position on the chromosome (Mb) and y-axis is the −log10P value of the SNP association with normal cytogenetics B-ALL. Filled colors indicate linkage disequilibrium (LD), as measured by r2, with the most significant SNP (shown in purple); red shows a high degree of LD whereas blue indicates lower r2. Meta-analyses show that the T allele (MAF = 0.07) increases odds of normal cytogenetic B-ALL by over 3.5-fold compared with controls (Pmeta = 5.6 × 10−9). This association was seen only with normal cytogenetic B-ALL and not observed in other subtypes. CPSF2 is the nearest gene to the association signal.

Regional plot of SNP associations with normal cytogenetic B-ALL. Regional plot showing association with normal cytogenetic B-ALL in a region of chromosome 14 (rs189434316). The x-axis is the position on the chromosome (Mb) and y-axis is the −log10P value of the SNP association with normal cytogenetics B-ALL. Filled colors indicate linkage disequilibrium (LD), as measured by r2, with the most significant SNP (shown in purple); red shows a high degree of LD whereas blue indicates lower r2. Meta-analyses show that the T allele (MAF = 0.07) increases odds of normal cytogenetic B-ALL by over 3.5-fold compared with controls (Pmeta = 5.6 × 10−9). This association was seen only with normal cytogenetic B-ALL and not observed in other subtypes. CPSF2 is the nearest gene to the association signal.

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