rs7193343
| Orientation | plus |
| Stabilized | plus |
| Make rs7193343(C;C) |
| Make rs7193343(C;T) |
| Make rs7193343(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 72995261 |
| Gene | ZFHX3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7193343 |
| dbSNP (classic) | rs7193343 |
| ClinGen | rs7193343 |
| ebi | rs7193343 |
| HLI | rs7193343 |
| Exac | rs7193343 |
| Gnomad | rs7193343 |
| Varsome | rs7193343 |
| LitVar | rs7193343 |
| Map | rs7193343 |
| PheGenI | rs7193343 |
| Biobank | rs7193343 |
| 1000 genomes | rs7193343 |
| hgdp | rs7193343 |
| ensembl | rs7193343 |
| geneview | rs7193343 |
| scholar | rs7193343 |
| rs7193343 | |
| pharmgkb | rs7193343 |
| gwascentral | rs7193343 |
| openSNP | rs7193343 |
| 23andMe | rs7193343 |
| SNPshot | rs7193343 |
| SNPdbe | rs7193343 |
| MSV3d | rs7193343 |
| GWAS Ctlg | rs7193343 |
| GMAF | 0.3118 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19597491
] and 23andMe blog report rs7193343(T)
- 1.2x odds of atrial fibrillation
- 1.1x odds of ischemic stroke
- 1.2x increased odds for cardioembolic stroke
but not significant among a Han Chinese population
[PMID 21107608] Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population
[PMID 21760908] Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population
[PMID 19132087] A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease.
[PMID 23428961] Common genetic polymorphism at 4q25 locus predicts atrial fibrillation recurrence after successful cardioversion.
[PMID 25325233] Linkage and Association Between Interleukin-6 Gene Polymorphisms and Ischemic Stroke: A Family-Based Study in the Northern Chinese Han Population
[PMID 25684755] Common Genetic Variants and Response to Atrial Fibrillation Ablation
[PMID 26112950] Rs7193343 polymorphism in zinc finger homeobox 3 (ZFHX3) gene and atrial fibrillation: an updated meta-analysis of 10 case-control comparisons
[PMID 26497660] Novel association of polymorphic genetic variants with predictors of outcome of catheter ablation in atrial fibrillation: new directions from a prospective study (DECAF)
[PMID 29624624] Genetic modulation of atrial fibrillation risk in a Hispanic/Latino cohort.
