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SNP information rs1800779


Normal allele: AA

Gene polymorphisms are associated with cardiovascular disease risk markers, impaired methylation.

Polymorphism rs1800779 is related to topics like this:

DNA methylation genes

The Genetic Methylation Check examines your DNA to offer insights into your unique methylation...

Mitochondria dna

The mitochondria contain circular chromosomes known as mitochondrial DNA and are organelles...

Research and publications:

  15726497   Gene-environment interaction effects on the development of immune responses in the 1st year of life

  18069999   Renin-angiotensin and endothelial nitric oxide synthase gene polymorphisms are not associated with the risk of incident type 2 diabetes mellitus: a prospective cohort study.

  18246059   Habitual energy expenditure modifies the association between NOS3 gene polymorphisms and blood pressure.

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

  18687083   Lack of association of endothelial nitric oxide synthase polymorphisms and migraine.

  18698212   Association of renin-angiotensin and endothelial nitric oxide synthase gene polymorphisms with blood pressure progression and incident hypertension: prospective cohort study.

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

  19263529   Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach

  19330901   Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study

  19419976   Endothelial nitric oxide synthase tagging single nucleotide polymorphisms and recovery from aneurysmal subarachnoid hemorrhage.

  19493349   118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects

  19559392   A candidate gene association study of 77 polymorphisms in migraine

  19584173   Kininogen gene (KNG) variation has a consistent effect on aldosterone response to antihypertensive drug therapy: the GERA study.

  19661472   Relation of candidate genes that encode for endothelial function to migraine and stroke: the Stroke Prevention in Young Women study.

  19815736   Endothelial nitric oxide synthase gene variants and primary open-angle glaucoma: interactions with sex and postmenopausal hormone use.

  19884647   Air pollution, obesity, genes and cellular adhesion molecules

  20031567   Assessing candidate inflammatory and thrombotic genes for venous thromboembolism risk: the Women's Genome Health Study.

  20409549   NOS3 gene polymorphisms are associated with risk markers of cardiovascular disease, and interact with omega-3 polyunsaturated fatty acids.

  20417488   Association of fetal inflammation and coagulation pathway gene polymorphisms with neurodevelopmental delay at age 2 years

  20577119   Pharmacogenetic association of hypertension candidate genes with fasting glucose in the GenHAT Study.

  21122033   Leukoaraiosis is associated with genes regulating blood-brain barrier homeostasis in ischaemic stroke patients.

  21254358   Nonsyndromic cleft lip and palate: CRISPLD genes and the folate gene pathway connection.

  21254359   Folate pathway and nonsyndromic cleft lip and palate.

  21291465   The association of genetic polymorphisms with cerebral palsy: a meta-analysis.

  21674837   Association of NOS3 tag polymorphisms with hypoxic-ischemic encephalopathy.

  21857382   Candidate genes and risk for CP: a population-based study.

  21868014   Mechanisms of statin-induced myalgia assessed by physiogenomic associations.

  21886581   Genetic Association Analysis of NOS3 and Methamphetamine-Induced Psychosis Among Japanese.

  22184326   Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase.

  22470539   Pharmacogenetic association of NOS3 variants with cardiovascular disease in patients with hypertension: the GenHAT study.

  22769019   Association of inflammatory gene polymorphisms with ischemic stroke in a Chinese Han population.

  23826716   Association analysis of nitric oxide synthases: NOS1, NOS2A and NOS3 genes, with multiple sclerosis.

  25140814   Association of NOS3 gene variants and clinical contributors of hypoxic-ischemic encephalopathy.

  26355258   An Inflammatory Polymorphisms Risk Scoring System for the Differentiation of Ischemic Stroke Subtypes.

  26437765   Angiogenesis related genes NOS3, CD14, MMP3 and IL4R are associated to VEGF gene expression and circulating levels in healthy adults.

  26670709   Are Immune Modulating Single Nucleotide Polymorphisms Associated with Necrotizing Enterocolitis?

  27114698   Association of NOS3 gene polymorphism with Beh├žet's disease but not with Vogt-Koyanagi-Harada syndrome in Han Chinese.

  27616475   Gene variants as risk factors for gastroschisis.

  28070505   The Association between NOS3 Gene Polymorphisms and Hypoxic-Ischemic Encephalopathy Susceptibility and Symptoms in Chinese Han Population.

  28685066   Association of nitric oxide synthase 3 gene polymorphism with the risk of type 2 diabetes.

  30202567   Genetic findings in sport-related concussions: potential for individualized medicine?

  33195260   Non-syndromic Cleft Palate: An Overview on Human Genetic and Environmental Risk Factors.

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