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. 2017 May 8;12(5):e0177421. doi: 10.1371/journal.pone.0177421

Table 3. Association results of SNPs in CDKN2A/B and B-hyperdiploid ALL and ETV6-RUNX1 ALL.

B-hyperdiploid ALL ETV6-RUNX1 ALL
Gene Genotype N (controls) N (cases) OR (CI 95%) P N (cases) OR (CI 95%) P
SNP (N = 330) (N = 54) (N = 37)
ANRIL AA 264 (80.2) 40 (74.1) Recessive 0.007a 22 (62.9) Dominant 0.024
rs2811712 AG 62 (18.8) 10 (18.5) 8.69 (1.89–40.0) (0.048) 12 (34.3) 2.4 (1.15–5.02)
GG 3 (0.9) 4 (7.4) 1 (2.9)
A 590 (91.2) 90 (90.7) 1.73 (0.98–3.05) 0.055 56 (80) 2.16 (1.14–4.1) 0.017
G 68 (8.8) 18 (9.3) 14 (20)
CDKN2A CC 217 (92.7) 39 (83) Dominant 0.048 28 (90.3) Dominant 0.64
rs3731249 CT 16 (6.8) 8 (17) 2.62 (1.06–6.48) 3 (9.7) 1.37 (0.38–4.96)
TT 1 (0.4) 0 0
C 450 (96.2) 86 (91.5) 2.32 (0.98–5.51) 0.55 59 (95.2) 1.27 (0.36–4.44) 0.70
T 18 (3.8) 8 (8.5) 3 (4.8)
CDKN2A GG 203 (79.6) 38 (70.4) Additive 0.06 23 (67.6) Dominant 0.12
rs2811709 AG 49 (19.2) 13 (24.1) 1.72 (0.98–3.01) 11 (32.4) 1.87 (0.86–4.07)
AA 3 (1.2) 3 (5.6) 0
G 455 (89.2) 89 (82.4) 1.76 (0.99–3.11) 0.05 57 (83.8) 1.59 (0.79–3.22) 0.19
A 55 (10.8) 19 (17.6) 11 (16.2)
CDKN2B, ANRIL TT 125 (38.1) 23 (42.6) Dominant 0.53 12 (34.3) Dominant 0.65
rs1063192 CT 162 (49.4) 24 (44.4) 0.83 (0.46–1.49) 17 (48.6) 1.18 (0.57–2.46)
CC 41 (12.5) 7 (13) 6 (17.1)
T 412 (62.8) 70 (64.8) 0.91 (0.59–1.4) 0.68 41 (58.8) 1.19 (0.72–1.97) 0.48
C 244 (37.2) 38 (35.2) 29 (41.4)
CDKN2A AA 246 (74.8) 41 (77.4) Dominant 0.68 27 (77.1) Dominant 0.75
rs3731222 AG 78 (23.7) 12 (22.6) 0.87 (0.44–1.73) 7 (20) 0.88 (0.38–2.01)
GG 5 (1.5) 0 1 (2.9)
A 570 (86.6) 94 (88.7) 0.82 (0.43–1.57) 0.56 61 (87.1) 0.95 (0.45–1.99) 0.90
G 88 (13.4) 12 (11.3) 9 (12.9)
CDKN2B, ANRIL GG 95 (28.9) 17 (31.5) Recessive 0.93 15 (44.1) Aditive 0.030
rs3217992 AG 153 (46.5) 24 (44.4) 0.97 (0.5–1.9) 15 (44.1) 0.58 (0.34–0.96)
AA 81 (24.6) 13 (24.1) 4 (11.8)
G 343 (52.1) 58 (53.7) 0.93 (0.62–1.41) 0.76 45 (66.2) 0.55 (0.32–0.94) 0.028
A 315 (47.9) 50 (46.3) 23 (33.8)

Abbreviations: CI, confidence interval; OR, odds ratio; SNP, single-nucleotide polymorphism

a Significant after FDR correction, the p value is displayed in brackets