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SNP information rs2288904

RS2288904

Normal allele: AA

The SLC44A2 rs2288904 variant is associated with the risk of recurrent venous thromboembolism.

Polymorphism rs2288904 is related to topics like this:

G20210A prothrombin mutation

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Research and publications:

  24236643   HNA-3 gene frequencies in Brazilians and a new polymerase chain reaction-restriction fragment length polymorphism method for HNA-3a/3b genotyping.

  26593331   Genotype frequency of human neutrophil antigen-3 polymorphisms in the Yi, Han, and Tibetan populations of China.

  26888256   Novel genetic predictors of venous thromboembolism risk in African Americans.

  27766050   Causes of venous thrombosis.

  27829169   Single nucleotide polymorphisms, isoforms and expression of SLC44A2: association with severity of Meniere's disease?

  29190926   Polymorphism of the ABO gene associate with thrombosis risk in patients with paroxysmal nocturnal hemoglobinuria.

  29540240   HNA-3a and HNA-3b antigens among 9 ethnic populations and the Han population in Southwest China.

  30634167   Association between SLC44A2 rs2288904 polymorphism and risk of recurrent venous thromboembolism among Thai patients.

  31420334   Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.

  31689458   Venous thromboembolism GWAS reported genetic makeup and the hallmarks of cancer: Linkage to ovarian tumour behaviour.

  32314961   Activated α(IIb)β(3) on platelets mediates flow-dependent NETosis via SLC44A2.

  32581188   The Effect of Common Variants in SLC44A2 on the Contribution to the Risk of Deep Cein Thrombosis after Orthopedic Surgery.

  35646052   SLC44A2 Frequency, a New TaqMan Real-Time Polymerase Chain Reaction Method for HNA-3A/3B Genotyping, and a New Application of Droplet Digital PCR.

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