|| >1.26x increased risk for heart disease
|| 1.26x increased risk for heart disease
|?|| (C;C) (C;T) (T;T) ||28|
is a SNP found to be associated with heart disease
by the German MI (Myocardial infarction) Family Study group in two populations. The odds ratio per allele is 1.26 (CI: 1.11-1.44, p=0.0178).[PMID 17634449
[PMID 18979498] rs599839, rs4970834 and rs17228212 associated with non-HDL cholesterol
[PMID 18780302] Association studies of 22 candidate SNPs with late-onset Alzheimer's disease.
[PMID 19198609] Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
[PMID 19750184] Genome-wide association studies for atherosclerotic vascular disease and its risk factors.
[PMID 19956433] Genetics of coronary artery disease: focus on genome-wide association studies.
[PMID 20017983] Evaluation of population impact of candidate polymorphisms for coronary heart disease in the Framingham Heart Study Offspring Cohort.
[PMID 20098575] Genetics and cardiovascular disease: Design and development of a DNA biobank.
[PMID 21804106] Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration.
[PMID 26110764] Characterization of SMAD3 Gene Variants for Possible Roles in Ventricular Septal Defects and Other Congenital Heart Diseases