Genome-wide significant SNPs associated with a variation in IL-10 levels.

All genome wide significant results from GWAS in ACS patients and controls separately. The table includes basic information on the original SNP name on the CardioMetaboChip, The RS number (SNP name), chromosome and position of the SNP. In addition, the table shows which allele the effect (Beta) was estimated for, the frequency of that allele and the effect (Beta) the allele have on IL-10 levels with corresponding standard error (SE) and P-value. The table also includes basic QC values for the SNPs including number of individuals successfully genotyped, SNP call rate, and Hardy-Weinberg equilibrium P-value (HWE P).Genome-wide significant SNPs associated with a variation in IL-10 levels.