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Table 2 The association between ANRIL ENST00000428597 and known CAD risk variants

From: The cis and trans effects of the risk variants of coronary artery disease in the Chr9p21 region

CAD risk SNP Risk allele Coded allele Non coded allele Coded allele frequency Parameter estimate SE P-value
rs7865618 A A G 0.569 0.070 0.0155 8.58e-06
rs10811650 G G A 0.490 0.043 0.0154 0.0058
rs1333040 T T C 0.605 0.028 0.0158 0.0755
rs10757274 G G A 0.490 0.030 0.0152 0.0522
rs2383206 G G A 0.504 0.033 0.0153 0.0345
rs1333045 C C T 0.543 0.030 0.0158 0.0588