abstract |
The present disclosure relates to a method of determining a risk of developing coronary artery disease in a subject, the method comprising identifying whether at least 95 single nucleotide polymorphisms (SNPs) from Table D is present in a biological sample from the subject, wherein the presence of a risk allele of a SNP from Table D indicates that the subject has an increased risk of coronary artery disease, and wherein the presence of an alternative allele indicates that the subject has a decreased risk of coronary artery disease. |