Nineteen established CRC risk variants identified by GWAS and their proxies considered in this study.
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aPosition based on dbSNP build 130. bMajor allele/minor allele among Europeans. cMinor allele frequencies from published reports. dLinkage disequilibrium between SNP and proxy in HapMap CEU. eNot on Affymetrix 6.0 array. fExcluded from analysis as proxy r2<0.90.
创建时间：
2012-02-17
