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. 2016 Apr 1;12(2):67–71. doi: 10.5152/tjbh.2016.2881

Table 1.

The genotype and allele frequencies of SNP 276G/T [BsmI (rs1501299)] and 45T/G [Smal (rs2241766)] in the breast cancer and control groups

Genotype Breast Cancer Patients Control Patients χ2 p OR; 95% CI
BsmI (rs1501299) 97 (100.0) 101 (100.0) 2.694 0.260
GG 44 (45.4) 56 (55.4) 2.013 0.156 0.667 (0.381 – 1.168)
GT 44 (45.4) 40 (39.6) 0.671 0.413 1.266 (0.720 – 2.227)
TT 9 (9.3) 5 (5.0) 1.410 0.235 1.964 (0.634 – 6.084)
Allele frequency
G 132 (68.1) 152 (75.24) 1.410 0.235 0.509 (0.164–1.578)
T 62 (32.0) 50 (24.75) 2.013 0.156 1.499 (0.856–2.625)
HWE (p) 0.816 0.789
Smal (rs2241766) 97 (100.0) 101 (100.0) 1.126 0.569
TT 60 (61.9) 68 (67.3) 0.648 0.421 0.787 (0.439–1.411)
TG 36 (37.1) 31 (30.7) 0.911 0.340 1.333 (0.738–2.405)
GG 1 (1.0) 2 (2.0) 0.299 0.585 0.516 (0.046–5.780)
Allele frequency
T 156 (80.4) 167 (82.7) 0.299 0.585 1.939 (0.173–21.741)
G 38 (19.6) 35 (17.3) 0.648 0.421 1.271 (0.709–2.278)
HWE (p) 0.110 0.730

HWE: Hardy-Weinberg Equation; OR: odds ratio; CI: confidence interval