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SNP information rs1165196

RS1165196

Normal allele: AA

Polymorphism rs1165196 is related to topics like this:

Genetic haemochromatosis

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

Research and publications:

  18834626   Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study.

  19556210   Sodium-dependent phosphate cotransporter type 1 sequence polymorphisms in male patients with gout.

  20583287   Analyze multivariate phenotypes in genetic association studies by combining univariate association tests.

  20884846   Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.

  22229870   Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia.

  22300439   The pharmacokinetics of oxypurinol in people with gout.

  22541845   The renal urate transporter SLC17A1 locus: confirmation of association with gout.

  22609445   Pathway analysis of genome-wide association studies on uric acid concentrations.

  25128519   Tubular urate transporter gene polymorphisms differentiate patients with gout who have normal and decreased urinary uric acid excretion.

  25252215   NPT1/SLC17A1 is a renal urate exporter in humans and its common gain-of-function variant decreases the risk of renal underexcretion gout.

  26524967   Genetic variants of SLC17A1 are associated with cholesterol homeostasis and hyperhomocysteinaemia in Japanese men.

  26902266   Genome wide association study of uric acid in Indian population and interaction of identified variants with Type 2 diabetes.

  30123371   Multiple Membrane Transporters and Some Immune Regulatory Genes are Major Genetic Factors to Gout.

  31884074   Circulating Levels of Insulin-like Growth Factor 1 and Insulin-like Growth Factor Binding Protein 3 Associate With Risk of Colorectal Cancer Based on Serologic and Mendelian Randomization Analyses.

  32375679   Deciphering genetic signatures by whole exome sequencing in a case of co-prevalence of severe renal hypouricemia and diabetes with impaired insulin secretion.

  32474920   A mendelian randomization analysis: The causal association between serum uric acid and atrial fibrillation.

  34204277   Modulation of Urate Transport by Drugs.

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...

CCNB1 cyclin B1

Cyclin B1 serves as a regulatory protein pivotal in the process of mitosis. It forms complexes with...

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