Normal allele: CC
Polymorphism rs12190287 is related to topics like this:
Research and publications:
21378990 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
21673312 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
21875899 Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour.
22588700 Genetics of coronary artery disease in the 21st century.
22589742 Genome-wide association of pericardial fat identifies a unique locus for ectopic fat.
24219970 Common genetic variants do not associate with CAD in familial hypercholesterolemia.
24475106 Genetic variants associated with myocardial infarction and the risk factors in Chinese population.
24932356 Genetics of coronary artery disease: an update.
25294186 Cohen to identify the connection of the disease with rare genetic variants.
25469254 Association of a genetic variant of the ZPR1 zinc finger gene with type 2 diabetes mellitus.
25469260 Association of a transcription factor 21 gene polymorphism with hypertension.
25473424 Enhancer variants: evaluating functions in common disease.
26293461 Prediction of Causal Candidate Genes in Coronary Artery Disease Loci.
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.
27270650 TCF21 genetic polymorphisms and breast cancer risk in Chinese women.
27294088 Genetics of the acute coronary syndrome.
27386823 Integrative functional genomics identifies regulatory mechanisms at coronary artery disease loci.
27888760 Relationship between selected DNA polymorphisms and coronary artery disease complications.
28686695 Coronary artery disease-associated genetic variants and biomarkers of inflammation.
29435029 Nucleotide variation in ATG4A and susceptibility to cervical cancer in Southwestern Chinese women.
30065929 Integrating Genes Affecting Coronary Artery Disease in Functional Networks by Multi-OMICs Approach.
30571812 Additional value of a combined genetic risk score to standard cardiovascular stratification.
31043074 Genetic Insights Into Smooth Muscle Cell Contributions to Coronary Artery Disease.
31845553 Precision Medicine and Cardiovascular Health: Insights from Mendelian Randomization Analyses.
32894086 MassARRAY-based single nucleotide polymorphism analysis in breast cancer of north Indian population.
34276231 Epicardial Adipose Tissue: The Genetics Behind an Emerging Cardiovascular Risk Marker.