Additional file 1: Table S1. of Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs
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Genome coordinates and reported ORs for the breast cancer risk SNPs used in this study. Table S2. Sequencing coverage of 56 candidate genes in case and control cohorts. Table S3. Rare (MAF, <â0.001) missense variants detected in case and control cohorts. Table S4. SNP and rare variant association analysis. (XLSX 111Â kb)
创建时间：
2018-01-10
