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SNP information rs579459

RS579459

Normal allele: TT

Polymorphism rs579459 is related to topics like this:

G20210A prothrombin mutation

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Heart disease genetic

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Stroke genes

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Genetic protein diet

Incorporating protein into your diet can aid in weight loss, and maintaining a high protein diet...


Research and publications:

  19729612   Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin.

  20167578   Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels.

  21239051   Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies.

  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.

  22001757   Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

  22010135   Association of variation at the ABO locus with circulating levels of soluble intercellular adhesion molecule-1, soluble P-selectin, and soluble E-selectin: a meta-analysis.

  22588700   Genetics of coronary artery disease in the 21st century.

  22963146   Association between the ABO locus and hematological traits in Korean.

  23133757   ABO Blood Groups and Cardiovascular Diseases.

  23161703   Influence of 23 coronary artery disease variants on recurrent myocardial infarction or cardiac death: the GRACE Genetics Study.

  23251661   Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population

  23468967   Improvement in prediction of coronary heart disease risk over conventional risk factors using SNPs identified in genome-wide association studies.

  24219970   Common genetic variants do not associate with CAD in familial hypercholesterolemia.

  24251769   LDL-c-linked SNPs are associated with LDL-c and myocardial infarction despite lipid-lowering therapy in patients with established vascular disease.

  24475106   Genetic variants associated with myocardial infarction and the risk factors in Chinese population.

  24745723   Influence of coronary artery disease-associated genetic variants on risk of venous thromboembolism.

  24922540   Genetic determinants of long-term changes in blood lipid concentrations: 10-year follow-up of the GLACIER study.

  24932356   Genetics of coronary artery disease: an update.

  25025429   Single nucleotide polymorphisms with cis-regulatory effects on long non-coding transcripts in human primary monocytes.

  25302496   Using multivariable Mendelian randomization to disentangle the causal effects of lipid fractions.

  25542012   Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE study.

  26232166   Utility of a genetic risk score to predict recurrent cardiovascular events 1 year after an acute coronary syndrome: A pooled analysis of the RISCA, PRAXY, and TRIUMPH cohorts.

  26413716   A GWAS Study on Liver Function Test Using eMERGE Network Participants.

  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.

  26950853   Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.

  26958643   Detailed analysis of association between common single nucleotide polymorphisms and subclinical atherosclerosis: The Multi-ethnic Study of Atherosclerosis.

  27187494   Case-Only Survival Analysis Reveals Unique Effects of Genotype, Sex, and Coronary Disease Severity on Survivorship.

  27189168   The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular disease.

  27280446   Replication and Characterization of Association between ABO SNPs and Red Blood Cell Traits by Meta-Analysis in Europeans.

  27294088   Genetics of the acute coronary syndrome.

  27424552   Genomics era and complex disorders: Implications of GWAS with special reference to coronary artery disease, type 2 diabetes mellitus, and cancers.

  27542834   Association study of polymorphisms in the ABO gene with ischemic stroke in the Chinese population.

  27696788   Coronary Artery Calcification and Rheumatoid Arthritis: Lack of Relationship to Risk Alleles for Coronary Artery Disease in the General Population.

  28209224   Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.

  28984382   Association study of polymorphisms in the ABO gene and their gene-gene interactions with ischemic stroke in Chinese population.

  29390587   Prospective association of a genetic risk score with major adverse cardiovascular events in patients with coronary artery disease.

  30653588   Adhesion molecule gene variants and plasma protein levels in patients with suspected obstructive sleep apnea.

  31420334   Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.

  31845553   Precision Medicine and Cardiovascular Health: Insights from Mendelian Randomization Analyses.

  32062209   Short-term exposure to air pollution and its interaction effects with two ABO SNPs on blood lipid levels in northern China: A family-based study.

  32084209   A genome-wide association study on liver enzymes in Korean population.

  35454075   The rs8176740 T/A and rs512770 T/C Genetic Variants of the ABO Gene Increased the Risk of COVID-19, as well as the Plasma Concentration Platelets.

  35672559   The rs579459 ABO gene polymorphism and risk of incident cardiovascular events in obstructive sleep apnea: a pilot study.

  35701116   [Interaction between ischemic stroke risk loci identified by genome-wide association studies and sleep habits].

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