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. 2019 Oct 18;10(25):6358–6363. doi: 10.7150/jca.37564

Table 1.

Associations between H19 polymorphisms and neuroblastoma susceptibility

Genotype Cases
(N=700)
Controls
(N=1514)
P a Crude OR
(95% CI)
P Adjusted OR
(95% CI) b
P b
rs2839698 G>A (HWE=0.406)
GG 331 (47.29) 704 (46.50) 1.00 1.00
AG 300 (42.86) 667 (44.06) 0.96 (0.79-1.16) 0.646 0.96 (0.79-1.16) 0.658
AA 69 (9.86) 143 (9.45) 1.03 (0.75-1.41) 0.871 1.04 (0.76-1.43) 0.805
Additive 0.858 0.99 (0.86-1.14) 0.900 1.00 (0.87-1.14) 0.956
Dominant 369 (52.71) 810 (53.50) 0.730 0.97 (0.81-1.16) 0.730 0.97 (0.81-1.16) 0.762
Recessive 631 (90.14) 1371 (90.55) 0.759 1.05 (0.78-1.42) 0.758 1.06 (0.79-1.44) 0.696
rs3024270 C>G (HWE=0.162)
CC 184 (26.29) 415 (27.41) 1.00 1.00
CG 362 (51.71) 781 (51.59) 1.05 (0.84-1.29) 0.684 1.05 (0.85-1.30) 0.679
GG 154 (22.00) 318 (21.00) 1.09 (0.84-1.42) 0.505 1.09 (0.84-1.42) 0.505
Additive 0.799 1.05 (0.92-1.19) 0.503 1.05 (0.92-1.19) 0.503
Dominant 516 (73.71) 1099 (72.59) 0.580 1.06 (0.87-1.30) 0.580 1.06 (0.87-1.30) 0.576
Recessive 546 (78.00) 1196 (79.00) 0.595 1.06 (0.85-1.32) 0.595 1.06 (0.85-1.32) 0.598
rs217727 G>A (HWE=0.744)
GG 331 (47.29) 679 (44.85) 1.00 1.00
AG 289 (41.29) 674 (44.52) 0.88 (0.73-1.06) 0.187 0.88 (0.72-1.06) 0.172
AA 80 (11.43) 161 (10.63) 1.02 (0.76-1.37) 0.900 1.02 (0.75-1.37) 0.922
Additive 0.359 0.96 (0.84-1.10) 0.591 0.96 (0.84-1.10) 0.561
Dominant 369 (52.71) 835 (55.15) 0.284 0.91 (0.76-1.09) 0.284 0.90 (0.75-1.08) 0.263
Recessive 620 (88.57) 1353 (89.37) 0.577 1.08 (0.82-1.44) 0.577 1.08 (0.81-1.44) 0.586
Combined effect of risk genotypes c
0 112 (16.00) 258 (17.04) 1.00 1.00
1 511 (73.00) 1109 (73.25) 1.06 (0.83-1.36) 0.634 1.06 (0.83-1.36) 0.643
2 77 (11.00) 147 (9.71) 1.21 (0.85-1.72) 0.298 1.22 (0.86-1.74) 0.272
1-2 588 (84.00) 1256 (82.96) 0.542 1.08 (0.85-1.37) 0.542 1.08 (0.85-1.38) 0.542

OR, odds ratio; CI, confidence interval; HWE, Hardy-Weinberg equilibrium. a χ2 test for genotype distributions between neuroblastoma patients and cancer-free controls. b Adjusted for age and gender. c Risk genotypes were carriers with rs2839698 AA, rs3024270 CG/GG and rs217727 AA genotypes.