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. 2010 Nov 8;10:613. doi: 10.1186/1471-2407-10-613

Table 6.

Haplotype distribution in patients and controls and association with breast cancer risk

Cases Controls
Haplotype N F N F OR 95%CI P χ2

AAGT 284 0.47 248 0.47 1
1 AAGC 72 0.12 63 0.12 0.99 0.68-1.45 0.92
GACC 60 0.1 48 0.09 1.09 0.72-1.62 0.68
AACC 54 0.09 42 0.08 1.12 0.72-1.73 0.65
GAGC 6 0.01 0 0 0.03*
Total 192 0.32 153 0.29 1.09 0.83-1.43 0.5
2 AGGT 66 0.11 53 0.1 1.08 0.72-1.62 0.68
AACT 30 0.05 26 0.05 1.00 0.58-1.75 1
GACT 24 0.04 26 0.05 0.80 0.45-1.44 0.46
AGCT 0 0 5 0.01 0.02*
GAGT 0 0 5 0.01 0.02*
Others 8 0.01 12 0.02 0.58 0.23-1.44 0.23
Total 128 0.21 127 0.24 0.88 0.65-1.18 0.4

Total 604 1 528 1

The haplotype combining the predominant alleles was used as a reference. Group 1 was formed by any haplotype containing the rs5275 C allele and group 2 included all the other haplotypes. The haplotypes with less than 1% frequency (Others) are not listed. The impact on breast cancer risk was calculated for the two groups, considering the Odds Ratio (OR) and the 95% Confidence Interval (95%CI) P: Pearson P-value; N: Number of haplotypes. F: Frequency of haplotypes. * Fisher Exact Probability Test (two-tailed). OR was not calculated because of N = 0.