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Table 6 Distribution of genotypes of 10 selected miRSNPs in cases and controls and their association with leukemia risk

From: Polymorphisms in microRNA target sites modulate risk of lymphoblastic and myeloid leukemias and affect microRNA binding

SNP

Genotype

Controls (n = 471)

ALL (n = 101)

AML (n = 87)

CML (n = 140)

n (%)

n (%)

AdjustedaOR (95% CI)

p value

n (%)

AdjustedbOR (95% CI)

p value

n (%)

AdjustedbOR (95% CI)

p value

Genetic model

(Corrected)

Genetic model

(Corrected)

Genetic model

(Corrected)

ABL1 _rs7457 C > T

CC

402 (85.3%)

86 (85.1%)

1.3174 (0.2688-6.4561)

0.7339

78 (89.7%)

0.5735 (0.2744-1.1984)

0.1392

111 (79.3%)

1.5191 (0.9371-2.4627)

0.0898

CT

62 (13.2%)

13 (12.9%)

recessive

(0.7858)

9 (10.3%)

additive

(0.5367)

27 (19.3%)

dominant

(0.2993)

TT

7 (1.5%)

2 (2%)

  

0 (0%)

  

2 (1.4%)

  

ARHGAP26 _rs187729 T > C

TT

110 (23.4%)

24 (23.75%)

1.0728 (0.6463-1.7807)

0.7858

26 (30.2%)

0.6946 (0.4173-

0.161

30 (21.4%)

1.6297 (1.0755-2.4695)

0.0213

CT

255 (54.1%)

53 (52.5%)

recessive

(0.7858)

40 (46.5%)

1.1562)

(0.5367)

65 (46.4%)

recessive

(0.123)

CC

106 (22.5%)

24 (23.75%)

  

20 (23.3%)

dominant

 

45 (32.2%)

  

ATM _rs227091 T > C

TT

151 (32.2%)

21 (22.6%)

1.6473 (0.9892-2.7430)

0.0551

27 (31%)

0.7452 (0.3866-1.4366)

0.3799

48 (34.3%)

0.9103 (0.6104-1.3573)

0.6446

CT

236 (50.3%)

52 (55.9%)

additive

(0.1377)

48 (55.2%)

recessive

(0.5922)

67 (47.9%)

dominant

(0.8057)

CC

82 (17.5%)

20 (12.5%)

  

12 (13.8%)

  

25 (17.8%)

  

ETV6 _rs1573613 T > C

TT

158 (33.7%)

35 (34.7%)

1.8994 (1.1606-3.1085)

0.0107

26 (30.2%)

1.2629 (0.7114-2.2421)

0.4254

44 (31.4%)

0.7416 (0.4325-1.2715)

0.2771

CT

229 (48.8%)

37 (36.6%)

recessive

(0.0356)

42 (48.9%)

recessive

(0.5922)

77 (55%)

recessive

(0.5542)

CC

82 (17.5%)

29 (28.7%)

  

18 (20.9%)

  

19 (13.6%)

  

IRF4 _rs1877176 G > A

GG

331 (70.3%)

75 (74.3%)

0.7758 (0.4792-1.2560)

0.3017

60 (69%)

1.4661 (0.4608-4.6649)

0.5170

101 (72.1%)

1.2897 (0.4478-3.7139)

0.6373

AG

127 (27%)

25 (24.7%)

additive

(0.3771)

23 (26.4%)

recessive

(0.5922)

34 (24.3%)

recessive

(0.8057)

AA

13 (2.7%)

1 (1%)

  

4 (4.6%)

  

5 (3.6%)

  

IRF8 _rs10514611 C > T

CC

280 (59.6%)

56 (56%)

2.1876 (0.9232-5.1836)

0.0753

50 (57.5%)

1.1150 (0.7093-1.7526)

0.6373

84 (60%)

2.4008 (1.1189-5.1514)

0.0246

CT

172 (36.6%)

36 (36%)

recessive

(0.1656)

33 (37.9%)

additive

(0.6373)

44 (31.4%)

recessive

(0.123)

TT

18 (3.8%)

8 (8%)

  

4 (4.6%)

  

12 (8.6%)

  

NBN _rs2735383 G > C

GG

184 (39.2%)

32 (31.7%)

1.4140 (0.9089-2.2000)

0.1245

40 (46.5%)

0.7450 (0.4678-1.1863)

0.2148

56 (40%)

1.0854 (0.6492-1.8147)

0.7548

CG

214 (45.5%)

50 (49.5%)

additive

(0.1778)

32 (37.2%)

dominant

(0.537)

61 (43.6%)

recessive

(0.8387)

CC

72 (15.3%)

19 (18.8%)

  

14 (16.3%)

  

23 (16.4%)

  

PML _rs9479 G > A

GG

113 (24%)

37 (36.6%)

0.5527 (0.3569-0.8560)

0.0079

30 (34.5%)

0.6055 (0.3778-0.9706)

0.0372

37 (26.4%)

0.7626 (0.4759-1.2221)

0.26

AG

246 (52.2%)

43 (42.6%)

additive

(0.0356)

39 (44.8%)

additive

(0.372)

76 (54.3%)

recessive

(0.5542)

AA

112 (23.8%)

21 (20.8%)

  

18 (20.7%)

  

27 (19.3%)

  

TLX1 _rs1051723 C > T

CC

224 (47.5%)

56 (56%)

0.7097 (0.4672-1.0782)

0.1081

38 (43.7%)

1.1586 (0.7294-1.8405)

0.533

66 (47.1%)

1.0198 (0.7076-1.4696)

0.9164

CT

208 (44.2%)

37 (37%)

additive

(0.1778)

43 (49.4%)

dominant

(0.5922)

62 (44.3%)

additive

(0.9164)

TT

39 (8.3%)

7 (7%)

  

6 (6.9%)

  

12 (8.6%)

  

TLX1 _rs2742038 C > T

CC

325 (69%)

61 (60.4%)

3.9718 (1.4314-11.0211)

0.0081

58 (66.7%)

1.9108 (0.5019-7.2750)

0.3424

97 (69.3%)

0.3696 (0.0464-2.9453)

0.3472

CT

137 (29.1%)

33 (32.7%)

recessive

(0.0356)

26 (29.9%)

recessive

(0.5922)

42 (30%)

recessive

(0.5787)

TT

9 (1.9%)

7 (6.9%)

  

3 (3.4%)

  

1 (0.7%)

  
  1. For each SNP the best genetic model is presented.
  2. OR, odds ratio; CI, 95% confidence interval. OR adjusted for asex and bsex and age. Statistically significant results are in bold. Genotype frequencies in italics deviate from the Hardy–Weinberg equilibrium. Benjamiani-Hochberg false discovery rate control was used to correct for multiple comparisons.