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. 2012 Jan 9;103(3):497–503. doi: 10.1111/j.1349-7006.2011.02168.x

Table 2.

 Genotype frequencies and log‐rank P values for VEGFA and VEGFR2 polymorphisms in patients with diffuse large B cell lymphoma

Gene ID no. Base change Genotype Log‐rank P for OS Log‐rank P for PFS MAF in healthy population
MAF HWE P Additive Dominant Recessive Additive Dominant Recessive Korean Asian European† African†
VEGFA rs699947 −2578C>A 0.226 0.997 0.429 0.629 0.194 0.530 0.485 0.464 0.340‡ 0.318 0.408 0.117
rs2010963 +405G>C 0.337 0.687 0.882 0.991 0.650 0.812 0.940 0.562 0.519§ 0.352 0.431 0.340
rs3025039 +936C>T 0.154 0.055 0.497 0.543 0.437 0.289 0.348 0.318 0.206§ 0.182 0.186 0.068
VEGFR2 rs1870377 +1416T>A 0.322 0.253 0.004 0.002 0.021 0.010 0.004 0.049 0.344 0.275 0.117
rs2305948 +1192G/A 0.121 0.463 0.966 0.823 0.929 0.997 0.968 0.953 0.078 0.067 0.292

In the reference sequence, the transcription start site was designated nt +1. †Information about polymorphism ID and MAF in other ethnic populations (Asian, European and African‐American) were obtained from the National Center for Biotechnology Information database (http://www.ncbi.nlm.nih.gov). ‡From reference 43. §From reference 44. HWE, Hardy–Weinberg equilibrium; ID, identification; MAF, minor allele frequency; OS, overall survival; PFS, progression‐free survival; VEGFA, vascular endothelial growth factor A; VEGFR2, vascular endothelial growth factor receptor 2.