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. 2020 Jul 1;10(7):2160–2173.

Table 1.

Three genetic variants as independent BC risk predictors obtained from stepwise logistic regression analysis in the DRIVE study

SNP1 Location MAF Category2 Frequency OR (95% CI)1 P 1
SNAI1 rs1047920_T 20q13.13 0.07 CC/CT/TT 45730/6957/276 0.93 (0.88-0.97) 0.0014
AMDHD1 rs11826_T 12q23.1 0.24 CC/CT/TT 30973/18993/2997 0.96 (0.93-0.98) 0.0020
CUBN rs3914238_T 10p13 0.38 CC/CT/TT 20752/24693/7518 1.04 (1.01-1.07) 0.0022
1

Stepwise logistic regression analysis included age, PC1, PC3, PC4, PC5, PC6, PC8, PC10, PC11, PC14, PC16, four previously published risk-associated SNPs (rs1323697, rs1264308, rs141308737 and rs1469412) in the same study by Jie Ge (PMID: 31026346) and 11 SNPs (rs3914238, rs1047920, rs7913144, rs7898138, rs11424438, rs2271464, rs77090490, rs4141977, rs11826, rs1800629 and rs1800628).

2

The most left-hand side “category” was used as the reference.

Note: there were 20 PCs in the combined datasets as listed in Supplementary Table 3, of which ten remained significant and were adjusted in the final stepwise logistic regression analysis. Abbreviations: AMDHD1, amidohydrolase domain containing 1; BC, breast cancer; CI, confidence interval; CUBN, cubilin; DRIVE, Discovery, Biology, and Risk of Inherited Variants in Breast Cancer; SNP, single nucleotide polymorphism; MAF, minor allele frequency; OR, odds ratio; SNAI1, snail family transcriptional repressor 1.