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Table 2 Allele and genotype frequencies, odds ratios, 95% confidence intervals and p-values for the SNP rs13230029.

From: High-throughput genotyping of a common deletion polymorphism disrupting the TRY6 gene and its association with breast cancer risk

rs13230029

Cases (%)

Controls (%)

OR (95% CI)

p-value

CC

136 (0.34)

159 (0.35)

1

 

CG

190 (0.48)

216 (0.48)

1.03 (0.76–1.39)

0.86

GG

71 (0.18)

79 (0.17)

1.05 (0.71–1.56)

0.81

G%

0.42

0.41

  
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BMC Genomic Data

ISSN: 2730-6844

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