Table 4.
Haplotype | Controls | All cases (p-value=0.48) | Serous invasive cases (p-value=0.50) |
||||
---|---|---|---|---|---|---|---|
Frequency | Frequency | Score | p-value | Frequency | Score | p-value | |
11110 | 0.398 | 0.371 | −1.687 | 0.09 | 0.361 | −1.958 | 0.05 |
00001 | 0.289 | 0.286 | 0.282 | 0.77 | 0.293 | 0.612 | 0.54 |
00000 | 0.221 | 0.251 | 1.500 | 0.13 | 0.246 | 1.180 | 0.24 |
00010 | 0.083 | 0.082 | −0.025 | 0.98 | 0.088 | 0.340 | 0.73 |
11010 | 0.003 | 0.003 | −0.092 | 0.93 | 0.003 | 0.305 | 0.76 |
00110 | 0.002 | 0.004 | 1.364 | 0.17 | 0.005 | 1.142 | 0.25 |
0 indicates major allele, and 1 indicates minor allele for rs5987515, rs5987724, rs5945971, rs1045761, and rs5945680; adjusted for age, study site, race, parity, region of residence, age at first live birth, oral contraceptive use, hormone therapy use, and body mass index.