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SNP information rs1800822

RS1800822

Normal allele: CC

Polymorphism rs1800822 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:

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

  16601883   Diagnosis and management of trimethylaminuria (FMO3 deficiency) in children.

  21206424   Novel polymorphisms associated with tacrolimus trough concentrations: results from a multicenter kidney transplant consortium.

  21791690   Germline mutations in MSR1, ASCC1, and CTHRC1 in patients with Barrett esophagus and esophageal adenocarcinoma.

  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.

  27535031   Genome-wide linkage and association analysis of cardiometabolic phenotypes in Hispanic Americans.

  28084894   Donors FMO3 polymorphisms affect tacrolimus elimination in Chinese liver transplant patients.

  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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