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. 2018 Dec 25;100(2):344–350. doi: 10.4269/ajtmh.18-0731

Table 4.

Association between SNPs of candidate genes and patients with CP in the study cohort

Gene SNP ID Group HWE Genotypic analysis P-value
pp pq qq
IL-10 rs3024496 EN 0.122 68 (0.64) 33 (0.31) 5 (0.05) 0.886
CP 67 (0.65) 29 (0.28) 7 (0.07)
C/T
IL-10 rs1800872 EN 0.151 37 (0.35) 44 (0.42) 25 (0.23) 0.415
A/C CP 29 (0.28) 48 (0.47) 26 (0.25)
IL-10RA rs3135932 EN 0.399 77 (0.73) 24 (0.23) 5 (0.05) 0.692
A/G CP 76 (0.74) 24 (0.23) 3 (0.03)
IL-10RB rs2834167 EN 0.012 46 (0.43) 49 (0.46) 11 (0.10) 0.131
A/G CP 33 (0.32) 57 (0.55) 13 (0.13)
PD-1 rs2227982 EN 0.488 93 (0.88) 11 (0.10) 2 (0.02) 0.939
C/T CP 89 (0.86) 13 (0.13) 1 (0.01)
PD-1 rs10204525 EN 0.115 76 (0.72) 28 (0.26) 2 (0.02) 0.296
A/G CP 68 (0.66) 31 (0.30) 4 (0.04)
PD-L1 rs4143815 EN 0.117 77 (0.73) 26 (0.24) 3 (0.03) 0.779
C/G CP 78 (0.76) 21 (0.20) 4 (0.04)
PD-L2 rs7854413 EN < 0.001 65 (0.61) 36 (0.34) 5 (0.05) 0.037
C/T CP 52 (0.50) 38 (0.37) 13 (0.13)

CP = chronic pathology; EN = endemic normal; HWE = Hardy–Weinberg equilibrium; SNP = single-nucleotide polymorphism. Bold values represent statistic significance between the EN individuals and CP patients for IL-10RB and PD-L2 SNPs. Genotype and allelic frequencies for IL-10 and PD-1 pathway gene polymorphisms among chronic pathology and control groups were studied using the HWE and association between the SNP and CP was determined.