Normal allele: CC
Polymorphism rs9982601 is related to topics like this:
Research and publications:
19956433 Genetics of coronary artery disease: focus on genome-wide association studies.
20440292 Early identification of cardiovascular risk using genomics and proteomics.
20835900 Genetics of diabetes complications.
21378990 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
21860704 Implications of discoveries from genome-wide association studies in current cardiovascular practice.
21875899 Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour.
22152955 Genetic susceptibility to coronary heart disease in type 2 diabetes: 3 independent studies.
22588700 Genetics of coronary artery disease in the 21st century.
22848412 Genetic markers enhance coronary risk prediction in men: the MORGAM prospective cohorts.
24219970 Common genetic variants do not associate with CAD in familial hypercholesterolemia.
24932356 Genetics of coronary artery disease: an update.
26847647 Experimental Biology for the Identification of Causal Pathways in Atherosclerosis.
26892960 From Loci to Biology: Functional Genomics of Genome-Wide Association for Coronary Disease.
27294088 Genetics of the acute coronary syndrome.
28458444 Functional Analysis of the Coronary Heart Disease Risk Locus on Chromosome 21q22.
28686695 Coronary artery disease-associated genetic variants and biomarkers of inflammation.
31845553 Precision Medicine and Cardiovascular Health: Insights from Mendelian Randomization Analyses.
32632093 A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine.