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SNP information rs7193343

RS7193343

Normal allele: CC

Polymorphism rs7193343 is related to topics like this:

Stroke genes

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


Research and publications:

  19132087   A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease.

  19597491   A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.

  20850564   R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation.

  21058051   New information on the genetics of stroke.

  21107608   Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population.

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

  21629240   Genetic susceptibility to ischemic stroke.

  21760908   Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population.

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

  23428961   Common genetic polymorphism at 4q25 locus predicts atrial fibrillation recurrence after successful cardioversion.

  25262128   Association between rs2200733 and rs7193343 genetic variants and atrial fibrillation in a Spanish population, and meta-analysis of previous studies.

  25325233   Linkage and association between interleukin-6 gene polymorphisms and ischemic stroke: a family-based study in the northern Chinese Han population.

  25684755   Common genetic variants and response to atrial fibrillation ablation.

  26112950   Rs7193343 polymorphism in zinc finger homeobox 3 (ZFHX3) gene and atrial fibrillation: an updated meta-analysis of 10 case-control comparisons.

  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?

  26925117   The 4q25, 1q21, and 16q22 polymorphisms and recurrence of atrial fibrillation after pulmonary vein isolation.

  27713600   Association of Single Nucleotide Polymorphisms with Atrial Fibrillation and the Outcome after Catheter Ablation.

  29624624   Genetic modulation of atrial fibrillation risk in a Hispanic/Latino cohort.

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

  30448967   Genotype-phenotype associations in atrial fibrillation: meta-analysis.

  31169720   Association between gene variants and the recurrence of atrial fibrillation: An updated meta-analysis.

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

  34889223   Association between the rs2106261 polymorphism in the zinc finger homeobox 3 gene and risk of atrial fibrillation: Evidence from a PRISMA-compliant meta-analysis.

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