Coronary Artery Disease (CAD) MetaGRS

A genomic risk score for coronary artery disease, consisting of 1.7 million SNPs in hg19 coordinates.<br><br><div>Update Feb 5, 2018: one variant which was not a biallelic SNP (rs58575809) has been removed from the score.</div><div><br></div><div><br></div><div><b>References</b></div><div><b><br></b></div><div>- bioRxiv preprint: Inouye, Abraham, et al, "<b>Genomic risk prediction of coronary artery disease in nearly 500,000 adults: implications for early screening and primary prevention</b>", <i>bioRxiv</i> 2018, https://doi.org/10.1101/250712</div><div><br></div><div>- Accepted version: Inouye, Abraham, et al, "<b>Genomic Risk Prediction of CAD in Nearly 500,000 Adults: Early Screening and Primary Prevention</b>", <i>Journal of the American College of Cardiology</i>, 2018;72:1883-1893, https://doi.org/10.1016/j.jacc.2018.07.079<br> </div><br>