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SNP information rs7767084

RS7767084

Normal allele: TT

Polymorphism rs7767084 is related to topics like this:

Heart attack genetic

Genetic predisposition, also referred to as familial predisposition, is a crucial risk factor for...

Heart disease genetic

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


Research and publications:

  19956433   Genetics of coronary artery disease: focus on genome-wide association studies.

  20601648   Lipoprotein(a) levels and long-term cardiovascular risk in the contemporary era of statin therapy.

  20729558   Improved prediction of cardiovascular disease based on a panel of single nucleotide polymorphisms identified through genome-wide association studies.

  21242481   Genetic risk score and risk of myocardial infarction in Hispanics.

  21305047   Variation in LPA is associated with Lp(a) levels in three populations from the Third National Health and Nutrition Examination Survey.

  21369780   Genome-wide association studies in atherosclerosis.

  21860704   Implications of discoveries from genome-wide association studies in current cardiovascular practice.

  22152955   Genetic susceptibility to coronary heart disease in type 2 diabetes: 3 independent studies.

  22848412   Genetic markers enhance coronary risk prediction in men: the MORGAM prospective cohorts.

  22882272   Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke.

  23036009   Lack of association between four SNPs in the SLC22A3-LPAL2-LPA gene cluster and coronary artery disease in a Chinese Han population: a case control study.

  23653095   Positive correlation between variants of lipid metabolism‑related genes and coronary heart disease.

  26896185   Human Genetics and the Causal Role of Lipoprotein(a) for Various Diseases.

  27091178   Sex-Specific Genetic Variants are Associated With Coronary Endothelial Dysfunction.

  27621937   A Case-Control Study of the Relationship Between SLC22A3-LPAL2-LPA Gene Cluster Polymorphism and Coronary Artery Disease in the Han Chinese Population.

  35379196   Analysis of 61 SNPs from the CAD specific genomic loci reveals unique set of SNPs as significant markers in the Southern Indian population of Hyderabad.

CGRP migraine

Migraine affects a significant portion of the adult population in most countries, with a higher...

Factor 5 blood clotting disorder

Thrombophilia, an increased tendency to form abnormal blood clots that can obstruct blood vessels,...

Memory genes

Despite being often overlooked, the brain possesses an impressive ability to restrict the creation...

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