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 |