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SNP information rs72552713

RS72552713

Normal allele: GG

Polymorphism rs72552713 is related to topics like this:

Genetic haemochromatosis

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


Research and publications:

  16702730   Genetic variation and haplotype structure of the ABC transporter gene ABCG2 in a Japanese population.

  20368174   Common defects of ABCG2, a high-capacity urate exporter, cause gout: a function-based genetic analysis in a Japanese population.

  22246505   Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior.

  22246507   ABCG2 null alleles define the Jr(a-) blood group phenotype.

  24532835   Joint effects of alcohol consumption and ABCG2 Q141K on chronic tophaceous gout risk.

  25515134   Sunitinib-induced severe toxicities in a Japanese patient with the ABCG2 421 AA genotype.

  25646370   Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes.

  27571712   Hyperuricemia in acute gastroenteritis is caused by decreased urate excretion via ABCG2.

  29193749   Clinical Implementation of Pharmacogenetic Testing in a Hospital of the Spanish National Health System: Strategy and Experience Over 3 Years.

  29225919   Multiple common and rare variants of ABCG2 cause gout.

  29342419   Investigation of the transport of xanthine dehydrogenase inhibitors by the urate transporter ABCG2.

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

  30621105   Polymorphisms of ABCG2 and SLC22A12 Genes Associated with Gout Risk in Vietnamese Population.

  32180207   Dysfunctional ABCG2 gene polymorphisms are associated with serum uric acid levels and all-cause mortality in hemodialysis patients.

  34009629   Porphyrin accumulation in humans with common dysfunctional variants of ABCG2, a porphyrin transporter: potential association with acquired photosensitivity.

  34703277   Pharmacokinetics of Tenofovir Alafenamide Fumarate and Tenofovir in the Chinese People: Effects of Non-Genetic Factors and Genetic Variations.

  35702613   Examining an Association of Single Nucleotide Polymorphisms with Hyperuricemia in Chinese Flight Attendants.

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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