Fig. 2.

Association between genetic variants of DAPK1 and TNFSF8 and lung cancer risk based on the data from the Texas lung cancer GWAS. (A) A total of 92 SNPs were assigned to DAPK1, which covered the gene region between 89 175 300 and 89 347 200 bp on chromosome 9. Only four SNPs had a P value <0.01 and two SNPs rs3128477 and rs721936 were in high LD (r² = 0.99). LD patterns among these SNPs were inferred in the control subjects by Haploview. (B) A total of 18 SNPs were assigned to TNFSF8, which covered the gene region between 116 660 000 and 116 780 000 bp on chromosome 9. Only three SNPs had a P value <0.01 and three SNPs were in high LD to each other (r² > 0.8). LD patterns among these SNPs were inferred in the control subjects by Haploview.