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Normal allele: GG
Polymorphism rs1736557 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...
While the body requires only minuscule quantities of the trace mineral molybdenum, it serves as a...
Research and publications:
11191884 Compound heterozygosity for missense mutations in the flavin-containing monooxygenase 3 (FM03) gene in patients with fish-odour syndrome.
12527699 Identification of novel variants of the flavin-containing monooxygenase gene family in African Americans.
15858076 Discovery of novel flavin-containing monooxygenase 3 (FMO3) single nucleotide polymorphisms and functional analysis of upstream haplotype variants.
17531949 Functional characterization of genetic variants of human FMO3 associated with trimethylaminuria.
22824134 Polymorphism in glutamate cysteine ligase catalytic subunit (GCLC) is associated with sulfamethoxazole-induced hypersensitivity in HIV/AIDS patients.
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.
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.
30814476 Novel Association between Flavin-Containing Monooxygenase 3 Gene Polymorphism and Antithyroid Drug-Induced Agranulocytosis in the Han Population.
Hereditary hemochromatosis is a genetic condition associated with severe liver disease and various...
We recommend that anyone who has been diagnosed with autism undergo genetic testing. Unfortunately,...
Lactose intolerance is a condition characterized by difficulty digesting lactose, a sugar present...