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Table 1 The risk associations between ARID5B rs10821936 genotype and MLL translocation partner genes or MLL breakpoint region, Brazil, 2003-2013

From: ARID5B polymorphism confers an increased risk to acquire specific MLL rearrangements in early childhood leukemia

 

Controls

MLLtranslocation partner genes

MLLbreakpoint regiona

   

MLL-AFF1(n = 44)

 

MLL-MLLT1(n = 21)

 

MLL-MLLT3(n = 17)

 

A (n = 15) and B (n = 8)

 

C (n = 18)

 

n

n

OR (95% CI)b,c

n

OR (95% CI)b,c

n

OR (95% CI)b,c

n

OR (95% CI)b,c

n

OR (95% CI)b,c

ARID5B

           

   rs10821936

           

   TT

200

11

1.00

6

1.00

2

1.00

2

1.00

5

1.00

   TC

205

27

3.26 (1.42-7.49)

11

2.82 (0.89-8.93)

12

8.62 (1.77-41.94)

17

12.76 (2.66-61.23)

12

3.45 (1.08-11.05)

   CC

68

6

1.95 (0.62-6.11)

4

2.12 (0.52-8.63)

3

5.18 (0.79-34.02)

4

6.65 (1.08-41.15)

1

0.85 (0.09-8.25)

   TC + CC

273

33

2.79 (1.27-6.11)

15

2.53 (0.89-7.22)

15

7.10 (1.54-32.68)

22

10.25 (2.24-46.81)

14

2.72 (0.88-8.43)

  1. n, number of individuals; OR, odds ratio; CI, confidence intervals; aThe MLL breakpoint region was subdivided according to Meyer et al., 201332 as follows: (A) Exon 9-Intron 9, (B) Exon 10-Intron 10, (C) Intron 11; bAdjusted on age; cAdjusted on skin color.