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Table 1 Top SNPs associated with each transcript

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

Transcript ID Top SNP Coded allele Non coded allele Coded allele frequency Parameter estimate SE P-value
ANRIL        
ENST00000428597 rs7865618 A G 0.569 0.07 0.016 8.58e-06
ENST00000422420 rs1759417 C T 0.834 -0.08 0.045 0.088
C9orf53        
ENST00000441769 rs662463 G A 0.896 0.07 0.024 0.006
CDKN2A        
ENST00000380151 rs647188 T G 0.891 -0.07 0.055 0.199
ENST00000361570 rs647188 T G 0.891 -0.07 0.045 0.121
ENST00000304494 rs647188 T G 0.891 -0.06 0.047 0.209
CDKN2B        
ENST00000380142 rs2095144 G A 0.707 0.03 0.012 0.030
ENST00000276925 rs1333040 T C 0.605 0.02 0.011 0.070