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. Author manuscript; available in PMC: 2015 Feb 1.
Published in final edited form as: Nat Genet. 2014 Jul 20;46(8):886–890. doi: 10.1038/ng.3041

Table 1.

Associations of breast cancer risk with newly identified risk variants: Results from the Asia Breast Cancer Consortium

SNP (Allelesa) Frequencyb Locus (Positionc) Closest gene (Annotation) Stage Per-allele association P for heterogeneityf
OR (95% CI)d Pe
rs4951011 (G/A) 0.282 1q32.1 (202,032,954) ZC3H11A (Intron 2) Stage 1 1.09 (1.02–1.17) 0.007
Stage 2 1.10 (1.02–1.18) 0.011
Stage 3 1.08 (1.05–1.12) 1.02 × 10−5
Combined 1.09 (1.06–1.12) 8.82 × 10−9 0.98
rs10474352 (C/T) 0.482 5q14.3 (90,767,981) ARRDC3 (Intergenic) Stage 1 1.09 (1.03–1.17) 0.006
Stage 2 1.12 (1.05–1.20) 7.06 × 10−4
Stage 3 1.08 (1.04–1.12) 1.92 × 10−5
Combined 1.09 (1.06–1.12) 1.67 × 10−9 0.50
rs2290203 (G/A) 0.504 15q26.1 (89,313,071) PRC1 (Intron 14) Stage 1 1.08 (1.02–1.14) 0.012
Stage 2 1.19 (1.10–1.30) 4.97 × 10−5
Stage 3 1.06 (1.03–1.10) 2.45 × 10−4
Combined 1.08 (1.05–1.11) 4.25 × 10−8 0.06

Abbreviations: OR, odds ratio; CI, confidence interval.

a

Risk/reference allele; risk allele is shown in bold.

b

Risk allele frequency in controls from all three stages combined.

c

Chromosome position (bp) based on NCBI Human Genome Build 36.

d

Per-allele OR (95% CI) was adjusted for age and principal components in each study; summary OR (95% CI) was obtained using fixed-effect meta-analysis in each stage.

e

Derived from a weighted z-statistic–based meta-analysis.

f

P for heterogeneity across studies in all stages was calculated using Cochran’s Q test.