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SNP information rs6843082

RS6843082

Normal allele: AA

Genetic risk factor for ischaemic and haemorrhagic stroke.

Polymorphism rs6843082 is related to topics like this:

Heart disease genetic

Although genetics can be a major factor in the development of certain heart diseases, individuals...

Stroke genes

Ischemic stroke has a multifactorial etiology, with genetic causes playing a significant role,...


Research and publications:

  20173747   Common variants in KCNN3 are associated with lone atrial fibrillation.

  21245058   Genome-wide association studies of atrial fibrillation: past, present, and future.

  22326711   There is power in numbers--even/especially in genomic medicine.

  22384221   Characterization of genome-wide association-identified variants for atrial fibrillation in African Americans.

  25711478   Association of GWAS-Supported Variants rs2200733 and rs6843082 on Chromosome 4q25 with Ischemic Stroke in the Southern Chinese Han Population.

  26272656   Korean Atrial Fibrillation (AF) Network: Genetic Variants for AF Do Not Predict Ablation Success.

  26497660   Novel association of polymorphic genetic variants with predictors of outcome of catheter ablation in atrial fibrillation: new directions from a prospective study (DECAF).

  26660272   Gene-guided therapy for catheter-ablation of atrial fibrillation: are we there yet?

  27185397   Exhaustive Genome-Wide Search for SNP-SNP Interactions Across 10 Human Diseases.

  27796860   Genetic Risk Factors for Ischemic and Hemorrhagic Stroke.

  29988284   A Chromosome 4q25 Variant is Associated with Atrial Fibrillation Recurrence After Catheter Ablation: A Systematic Review and Meta-Analysis.

  30182779   Genetic susceptibility to cerebrovascular disease: A systematic review.

  30808078   A Genetic Risk Score for Atrial Fibrillation Predicts the Response to Catheter Ablation.

  31757599   Ischemic Stroke and Genetic Variants: In Search of Association with Severity and Recurrence in a Brazilian Population.

  33284871   Personalized warfarin treatment based on the PITX2 single nucleotide polymorphism rs6843082.

  33350184   The Effects of Single Nucleotide Polymorphisms in Korean Patients with Early-onset Atrial Fibrillation after Catheter Ablation.

  36061199   Variants rs2200733 and rs6843082 Show Different Associations in Asian and Non-Asian Populations With Ischemic Stroke.

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