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. 2021 Mar 3;22(5):2535. doi: 10.3390/ijms22052535

Table 5.

Associations with breast cancer risk after adjustment for rs2346018 carrier probabilities a.

CpG Chromosome Position ∆l a Not Adjusted for SNPs b Adjusted for rs2346018
Biased HR (95% CI) c p-Value Biased HR (95% CI) c p-Value
cg06536614 5 135416381 143.6 3.1 (2.1–4.6) 7 × 10−9 3.0 (2.0–4.3) 3 × 10−8
cg00124993 5 135416412 108.0 3.2 (2.2–4.7) 2 × 10−8 3.0 (2.0–4.4) 9 × 10−8
cg26328633 5 135416394 107.5 3.2 (2.2–4.8) 2 × 10−8 3.0 (2.0–4.5) 4 × 10−8
cg25340688 5 135416398 105.9 3.2 (2.1–4.7) 3 × 10−8 2.9 (2.0–4.3) 1 × 10−7
cg26896946 5 135416405 92.1 3.6 (2.4–5.4) 2 × 10−9 3.3 (2.2–5.0) 8 × 10−9

a ∆l: heritability metric: details of the methods used to calculate the heritability metric, carrier probabilities and Cox models for association with breast cancer risk are provided in [1]. b These are published and unpublished results from our study Joo et al., 2018 [1] and are presented here for comparison with the results adjusted for rs2346018. c While p values are unbiased, hazard ratios are biased by the ascertainment of families for this study [1], and the HR estimates are only included here to show that they are virtually unchanged by adjustment for rs2346018.