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. Author manuscript; available in PMC: 2009 Dec 2.
Published in final edited form as: Leuk Res. 2008 Aug 8;33(2):250–258. doi: 10.1016/j.leukres.2008.06.031

Table 3.

CYP1A1 single nucleotide polymorphisms (SNPs) and childhood leukemia risk

All leukemia
ALL
Controls (n = 164) Cases (n = 164) OR (95% CI)a Cases (n = 106) OR (95% CI)a
–17961T>C
    CC 81 (50.0) 68 (43.3) Ref. 40 (39.2) Ref.
    CT 61 (37.7) 66 (42.0) 1.3 (0.8–2.1) 49 (48.0) 1.6 (0.9–2.8)
    TT 20 (12.3) 23 (14.7) 1.3 (0.7–2.8) 13 (12.8) 1.4 (0.6–3.1)
    CT/TT 81 (50.0) 89 (56.7) 1.3 (0.8–2.1) 62 (60.9) 1.6 (0.9–2.6)
–9893G>A
    GG 87 (54.4) 90 (57.0) Ref. 59 (58.4) Ref.
    GA 64 (40.0) 59 (37.3) 0.9 (0.6–1.4) 36 (35.6) 0.8 (0.5–1.4)
    AA 9 (5.6) 9 (5.7) 1.0 (0.4–2.8) 6 (5.9) 1.0 (0.3–3.0)
    GA/AA 73 (45.6) 68 (43.0) 0.9 (0.6–1.4) 42 (41.6) 0.8 (0.5–1.4)
Ex7+131A>G (I462V)
    AA 85 (53.5) 90 (56.3) Ref. 60 (57.1) Ref.
    AG 65 (40.9) 61 (38.1) 0.9 (0.5–1.4) 39 (37.1) 0.9 (0.5–1.5)
    GG 9 (5.7) 9 (5.6) 1.0 (0.4–2.7) 6 (5.7) 0.9 (0.3–2.7)
    AG/GG 74 (46.5) 70 (43.8) 0.9 (0.6–1.4) 45 (42.9) 0.9 (0.5–1.5)
1188C>T
    TT 56 (34.6) 58 (36.2) Ref. 34 (33.3) Ref.
    TC 74 (45.6) 80 (50.0) 0.9 (0.6–1.6) 56 (54.9) 1.1 (0.6–2.0)
    CC 32 (19.8) 22 (13.8) 0.7 (0.3–1.3) 12 (11.8) 0.6 (0.3–1.3)
    TC/CC 106 (65.4) 102 (63.8) 0.9 (0.5–1.4) 68 (66.7) 1.0 (0.6–1.7)
11599C>G
    CC 53 (32.5) 39 (24.4) Ref. 25 (24.3) Ref.
    CG 69 (42.3) 80 (50.0) 1.6 (0.9–2.8) 54 (52.4) 1.8 (1.0–3.3)
    GG 41 (25.2) 41 (25.6) 1.4 (0.7–2.5) 24 (23.3) 1.3 (0.6–2.7)
    CG/GG 110 (67.5) 121 (75.6) 1.5 (0.9–2.5) 78 (75.7) 1.6 (0.9–2.8)
Haplotypeb All leukemia
ALL
Controls (%) Cases (%) OR (95% CI)a Cases (%) OR (95% CI)a
TGATG 29.5 34.4 Ref. 35.2 Ref.
CAGCC 23.8 22.0 0.8 (0.5–1.2) 21.4 0.7 (0.4–1.2)
CGATG 17.9 16.6 0.8 (0.5–1.4) 14.8 0.7 (0.4–1.3)
CGACC 14.7 12.1 0.7 (0.4–1.2) 12.2 0.6 (0.3–1.2)
CGATC 10.9 11.4 1.0 (0.5–1.7) 12.2 0.9 (0.5–1.7)
Rare haplotypes 3.2 3.5 4.2
Pomnibusc 0.61 0.46
a

Adjusted for age of child, gender, father's education, and birth weight.

b

Composed of –17961T>C, –9893G>A, Ex7+13A>G (I462V), 1188C>T, and 11599C>G.

c

Omnibus test for overall distribution of haplotypes.