Table 1. Associations between variants of FGFR2, NCOA7, and EGFR and breast cancer risk: NBC, and CGEMS.
Each table row for a given gene presents a haplotype/allele for which tests of association were concordantly significant in the NBC and CGEMS study populations. The underlined SNP of EGFR was not genotyped in the CGEMS study, but was imputed with probability 0.79.