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SNP information rs10953541

RS10953541

Normal allele: TT

Polymorphism rs10953541 is related to topics like this:

Heart disease genetic

Although genetics can be a major factor in the development of certain heart diseases, individuals...


Research and publications:

  21068099   Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22.

  21846871   A genome-wide association study in europeans and South asians identifies 5 new 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.

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

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

  24825461   Genetic influences on hand osteoarthritis in Finnish women--a replication study of candidate genes.

  24932356   Genetics of coronary artery disease: an update.

  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.

  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.

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

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

  27294088   Genetics of the acute coronary syndrome.

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

  28686695   Coronary artery disease-associated genetic variants and biomarkers of inflammation.

  29695241   Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.

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

Hereditary sarcoma

Ewing sarcoma is a malignant growth that can manifest in either bones or soft tissues, such as...

Genetic testing for thyroid cancer

Thyroid cancer is a prevalent type of malignancy in the endocrine system. Children who undergo...

Depression is it genetic

Depression, also referred to as major depression or major depressive disorder, is a psychiatric...

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