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. Author manuscript; available in PMC: 2011 Apr 1.
Published in final edited form as: Cancer Res. 2010 Mar 23;70(7):2789–2798. doi: 10.1158/0008-5472.CAN-09-3541

Table 1.

Established Common Breast-Cancer Susceptibility SNPs proven to affect miRNA binding.

SNP Gene Location Chromosome Population No. of cases/controls Ref Notes Genotype and BC risk Odds Ratio (95% CI; p)
rs1982073 (T+29C) TGFB1 Exonic (missense; Leu10Pro) 19(q13.2) European (Netherlands) 143/3,646 [27] CC-carriers have increased risk of BC 1.4 (1.1–2.0; p=0.04)
European 3,987/3,867 [28] TGFB1 Pro variant is more highly secreted by cells CC vs T-carriers (Pro/Pro vs Leu-carriers) have increased BC risk 1.21 (1.05–1.37; p= 0.01)
rs1799782 (580C>T) XRCC1 Exonic (missense; Arg194Trp) 19(q13.31) Mixed ethnicity (Meta-analysis) 4,933/6,775 [22] Breast cancer together with other cancers TT+CT vs CC-carriers (Trp/Trp+Arg/Trp vs Arg/Arg-carriers) have lower BC risk 0.89 (0.81–0.98)
Mixed ethnicity (Nurses’ Health Study) 1,004/1,385 [35] Association with Breast cancer risk and carotenoids levels Trp-carriers have a marginal lower risk of BC and a definitely lower risk in association with high carotenoids levels 0.79(0.60–1.04) alone and 0.32 (0.16–0.61; p=0.003) with high carotenoids levels
American 502/502 [36] Postmenopausal women Trp-carriers among postmenopausal women have lower BC risk 0.62 (0.40–0.95; p<0.05)