Table S5 from Predicting Cancer Risk from Germline Whole-exome Sequencing Data Using a Novel Context-based Variant Aggregation Approach

Table S5: Significant predictors from individual association analyses based on SNP array data. The significance threshold for each cancer type was 0.05/2824 (2824 predictors were tested for each cancer type).

表 S5：基于单核苷酸多态性（SNP）芯片数据进行的个体关联分析中的显著预测因子。每种癌症类型的显著性阈值均为 0.05/2824（针对每种癌症类型，共测试了 2824 个预测因子）。