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SNP information rs2266780

RS2266780

Normal allele: AA

Polymorphism rs2266780 is related to topics like this:

Molybdenum supplement benefits

While the body requires only minuscule quantities of the trace mineral molybdenum, it serves as a...

Research and publications:

  9536088   Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication.

  10479479   Trimethylaminuria is caused by mutations of the FMO3 gene in a North American cohort.

  10485731   Mild trimethylaminuria caused by common variants in FMO3 gene.

  10896299   Biochemical and molecular studies in mild flavin monooxygenase 3 deficiency.

  11809920   Human hepatic flavin-containing monooxygenases 1 (FMO1) and 3 (FMO3) developmental expression.

  15858076   Discovery of novel flavin-containing monooxygenase 3 (FMO3) single nucleotide polymorphisms and functional analysis of upstream haplotype variants.

  18565990   Systematic biological prioritization after a genome-wide association study: an application to nicotine dependence

  20301282   Primary Trimethylaminuria.

  22409263   Flavin-containing monooxygenase 3 gene polymorphisms in Turkish population.

  22871999   Concordance of DMET plus genotyping results with those of orthogonal genotyping methods.

  23820649   Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease

  24165757   The association of cytochrome P450 genetic polymorphisms with sulfolane formation and the efficacy of a busulfan-based conditioning regimen in pediatric patients undergoing hematopoietic stem cell transplantation.

  24173915   Effects of single-nucleotide polymorphisms of FMO3 and FMO6 genes on pharmacokinetic characteristics of sulindac sulfide in premature labor.

  25741868   Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

  27513517   Association of FMO3 Variants and Trimethylamine N-Oxide Concentration, Disease Progression, and Mortality in CKD Patients.

  28290528   Nicotine dependence is associated with functional variation in FMO3, an enzyme that metabolizes nicotine in the brain.

  28819071   Genetic and Nongenetic Factors Associated with Protein Abundance of Flavin-Containing Monooxygenase 3 in Human Liver.

  29795455   Minor diplotypes of FMO3 might protect children and adolescents from obesity and insulin resistance.

  31932875   Variability of voriconazole concentrations in patients with hematopoietic stem cell transplantation and hematological malignancies: influence of loading dose, procalcitonin, and pregnane X receptor polymorphisms.

  34512362   Influence of FMO3 and CYP3A4 Polymorphisms on the Pharmacokinetics of Teneligliptin in Humans.

Genetic haemochromatosis

Hereditary hemochromatosis is a genetic condition associated with severe liver disease and various...

DNA test for autism

We recommend that anyone who has been diagnosed with autism undergo genetic testing. Unfortunately,...

Gene for lactose intolerance

Lactose intolerance is a condition characterized by difficulty digesting lactose, a sugar present...

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