Normal allele: TT
Polymorphism rs6725887 is related to topics like this:
Research and publications:
19812545 Origins and functional impact of copy number variation in the human genome.
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.
21304891 A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.
21369780 Genome-wide association studies in atherosclerosis.
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.
22216278 Large scale association analysis identifies three susceptibility loci for coronary artery disease.
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.
25469254 Association of a genetic variant of the ZPR1 zinc finger gene with type 2 diabetes mellitus.
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.
28686695 Coronary artery disease-associated genetic variants and biomarkers of inflammation.
31845553 Precision Medicine and Cardiovascular Health: Insights from Mendelian Randomization Analyses.