Coronary Heart Disease


[PMID 4021556] Analysis of common and coding variants with cardiovascular disease in the diabetes heart study.

[PMID 3584137] Improvement in Prediction of Coronary Heart Disease Risk over Conventional Risk Factors Using SNPs Identified in Genome-Wide Association Studies.

[PMID 3583714] Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study

[PMID 3266236] Genetic Profiling Using Genome-Wide Significant Coronary Artery Disease Risk Variants Does Not Improve the Prediction of Subclinical Atherosclerosis: The Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey – A Meta-Analysis of Three Independent Studies

[PMID 3179381] Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour.

[PMID 3178591] Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease.

[PMID 24573017] Associations between the CDKN2A/B, ADTRP and PDGFD Polymorphisms and the Development of Coronary Atherosclerosis in Japanese Patients.

[PMID 23202125] Large-scale association analysis identifies new risk loci for coronary artery disease.

rs4773144

Parent Gene: COL4A1, COL4A2

Importance: 3
Less common allele: G = 40%
More common allele: A = 60%
My Genotype: Log In
Risk Allele: G, G

Disease/Trait: Coronary Heart Disease

The G allele of rs4773144 is reported to be associated with Coronary Heart Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Coronary heart disease.

Disease/Trait: Coronary Heart Disease

The G allele of rs4773144 is reported to be associated with Coronary Heart Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Coronary artery disease.