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. 2010 Jun 24;6(6):e1001002. doi: 10.1371/journal.pgen.1001002

Table 5. Association of rs4784227 and the three previously-reported SNPs at 16q12with breast cancer risk among European American women.

Tested SNP a Study SNPs Adjusted No of cases No of controls Frequencyb OR (95% CI) P for trend
rs4784227 CGEMS None 1145 1142 0.29/0.25 1.17(1.03–1.34) 0.016
NBHS None 1357 1148 0.28/0.25 1.21(1.07–1.37) 0.003
rs3803662 CGEMS None 1145 1142 0.3/0.27 1.13(0.99–1.28) 0.06
NBHS None 1615 1467 0.31/0.27 1.22(1.09–1.36) 4.0×10−4
rs8051542 NBHS None 1587 1439 0.46/0.44 1.07(0.97–1.19) 0.18
rs12443621 CGEMS None 1145 1142 0.50/0.49 1.02(0.91–1.15) 0.70
rs4784227 NBHS rs8051542 1263 1080 0.28/0.25 1.22(1.06–1.40) 0.007
rs4784227 CGEMS rs12443621 1145 1142 0.29/0.25 1.25(1.06–1.47) 0.007
rs4784227 Both rs3803662 2431 2243 0.29/0.25 1.22(0.94–1.59) 0.13
rs8051542 NBHS rs4784227 1263 1080 0.45/0.44 0.98(0.86–1.11) 0.74
rs12443621 CGEMS rs4784227 1145 1142 0.50/0.49 0.91(0.79–1.05) 0.19
rs3803662 Both rs4784227 2431 2243 0.31/0.27 0.97(0.75–1.25) 0.82

a In CGEMS, data on rs8051542 was not available, and In NBHS data on for rs12443621 was not available.

b Risk allele frequency in cases/controls. Risk/reference alleles (based on forward strand) are T/C for rs8051542 and rs4784227 and A/G for rs12443621 and rs3803662.