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SNP information rs2622604

RS2622604

Normal allele: TT

Polymorphism rs2622604 is related to topics like this:

Genetic haemochromatosis

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

Research and publications:

  19696792   Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppression.

  22912756   Early sorafenib-induced toxicity is associated with drug exposure and UGTIA9 genetic polymorphism in patients with solid tumors: a preliminary study.

  24944790   Screening for 392 polymorphisms in 141 pharmacogenes.

  25110414   Pharmacogenetics research on chemotherapy resistance in colorectal cancer over the last 20 years.

  26001650   A case of metastatic renal cell carcinoma and bile duct carcinoma treated with a combination of sunitinib and gemcitabine.

  26369774   Impact of New Genomic Technologies on Understanding Adverse Drug Reactions.

  26830973   The influence of genetic variants of sorafenib on clinical outcomes and toxic effects in patients with advanced renal cell carcinoma.

  27787353   Modelling of atorvastatin pharmacokinetics and the identification of the effect of a BCRP polymorphism in the Japanese population.

  28289864   Correlation between clinical response to sorafenib in hepatocellular carcinoma treatment and polymorphisms of P-glycoprotein (ABCB1) and of breast cancer resistance protein (ABCG2): monocentric study.

  30068618   Cohort Profile: the Predictors of Breast Cancer Recurrence (ProBe CaRE) Premenopausal Breast Cancer Cohort Study in Denmark.

  32457635   Polymorphisms of Drug-Metabolizing Enzymes and Transporters Contribute to the Individual Variations of Erlotinib Steady State Trough Concentration, Treatment Outcomes, and Adverse Reactions in Epidermal Growth Factor Receptor-Mutated Non-Small C

  32639515   Bayesian Pathway Analysis for Complex Interactions.

  32780457   Pharmacogenetics for severe adverse drug reactions induced by molecular-targeted therapy.

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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