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SNP information rs268

Normal allele: AA

A break in the LPL lipoprotein lipase gene causes a 3-fold increased risk of idiopathic venous thromboembolism.

Polymorphism rs268 is related to topics like this:

The Prothrombin G20210A mutation, also known as Factor II mutation, is a hereditary trait that...

Research and publications:

  8541837   A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidemia.

  17357073   Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol

  18513389   New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background

  18660489   Multiple genetic variants along candidate pathways influence plasma high-density lipoprotein cholesterol concentrations.

  18922999   Seven lipoprotein lipase gene polymorphisms, lipid fractions, and coronary disease: a HuGE association review and meta-analysis.

  19041386   Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.

  19131662   A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients

  19489872   Association of polymorphisms in genes involved in lipoprotein metabolism with plasma concentrations of remnant lipoproteins and HDL subpopulations before and after hormone therapy in postmenopausal women.

  19501493   A composite scoring of genotypes discriminates coronary heart disease risk beyond conventional risk factors in the Boston Puerto Rican Health Study

  19602472   Lipid and endothelium-related genes, ambient particulate matter, and heart rate variability--the VA Normative Aging Study

  20421590   Genetic causes of high and low serum HDL-cholesterol.

  20429872   Additive effects of LPL, APOA5 and APOE variant combinations on triglyceride levels and hypertriglyceridemia: results of the ICARIA genetic sub-study

  20565774   Population based allele frequencies of disease associated polymorphisms in the Personalized Medicine Research Project

  20650961   Application of statistical and functional methodologies for the investigation of genetic determinants of coronary heart disease biomarkers: lipoprotein lipase genotype and plasma triglycerides as an exemplar.

  21767357   Genetic variants in lipid metabolism are independently associated with multiple features of the metabolic syndrome.

  22024213   A novel gene-environment interaction involved in endometriosis

  22042884   Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study.

  22239554   Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia.

  22629316   Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project.

  24319689   The roles of genetic polymorphisms and human immunodeficiency virus infection in lipid metabolism.

  25361584   Subgroups at high risk for ischaemic heart disease:identification and validation in 67‚ÄČ000 individuals from the general population.

  25474356   Highly significant association between two common single nucleotide polymorphisms in CORIN gene and preeclampsia in Caucasian women.

  25626708   Resequencing of LPL in African Blacks and associations with lipoprotein-lipid levels.

  30140409   Lipoprotein lipase gene polymorphisms as risk factors for stroke: a computational and meta-analysis.

  30333156   Genetic and secondary causes of severe HDL deficiency and cardiovascular disease.

  32952508   Association of Four Missense SNPs with Preeclampsia in Saudi Women.

  35351696   Empowering consumers to PREVENT diet-related diseases through OMICS sciences (PREVENTOMICS): protocol for a parallel double-blinded randomised intervention trial to investigate biomarker-based nutrition plans for weight loss.

A psychosis known as schizophrenia impacts an individual's thinking, sense of self, and...

ADHD, a behavioral disorder that usually commences during childhood, is marked by a brief attention...

Numerous gastrointestinal disorders exhibit an inherited nature or entail a genetic predisposition...