{{Rsnum
|rsid=2106261
|Gene=ZFHX3
|Chromosome=16
|position=73017721
|Orientation=minus
|GMAF=0.2287
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ZFHX3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 2.7 | 31.0 | 66.4
| HCB | 14.6 | 38.0 | 47.4
| JPT | 7.1 | 38.4 | 54.5
| YRI | 9.5 | 46.3 | 44.2
| ASW | 1.8 | 38.6 | 59.6
| CHB | 14.6 | 38.0 | 47.4
| CHD | 4.6 | 43.1 | 52.3
| GIH | 4.0 | 28.7 | 67.3
| LWK | 6.4 | 32.7 | 60.9
| MEX | 5.2 | 36.2 | 58.6
| MKK | 1.3 | 20.6 | 78.1
| TSI | 2.9 | 27.5 | 69.6
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19597492
|Trait=Atrial fibrillation
|Title=Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
|RiskAllele=T
|Pval=2E-15
|OR=1.25
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=20586826
|Title=The P-Selectin Gene Polymorphism Val168Met: A Novel Risk Marker for the Occurrence of Primary Ventricular Fibrillation During Acute Myocardial Infarction
}}

{{PharmGKB
|RSID=rs2106261
|Name_s=
|Gene_s=ZFHX3
|Feature=
|Evidence=PubMed ID:20173747
|Annotation=Risk or phenotype-associated allele: minor allele . Phenotype: This variant is associated with lone atrial fibrillation. Study size: 1,335 cases; 12,844 referants. Study population/ethnicity: Cases-German AF Network, Heart and Vascular Health Study, the Cleveland Clinic and Massachusetts General Hospital. Significance metric(s): OR (for each additional minor allele) = 1.47, 95% CI = 1.39 -1.54, P = 1.61 x 10(-7) . Type of association: CO;GN
|Drugs=
|Drug Classes=
|Diseases=Atrial Fibrillation
|Curation Level=Curated
|PharmGKB Accession ID=PA165291544
}}
{{PMID Auto
|PMID=21107608
|Title=Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population
}}

{{omim
|id=613055
|rsnum=2106261
}}

{{PMID Auto
|PMID=22690879
|Title=Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis
|OA=1
}}

{{PMID Auto GWAS
|PMID=22544366
|Trait=None
|Title=Meta-analysis identifies six new susceptibility loci for atrial fibrillation.
|RiskAllele=T
|Pval=3E-16
|OR=1.2400
|ORtxt=None
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2106261
|overall_frequency_n=36
|overall_frequency_d=128
|overall_frequency=0.28125
|n_genomes=30
|n_genomes_annotated=0
|n_haplomes=34
|n_articles=1
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{PMID Auto
|PMID=23132824
|Title=Genetic polymorphisms confer risk of atrial fibrillation in patients with heart failure: a population-based study
|OA=1
}}

{{PMID Auto
|PMID=24983873
|Title=Genetic Polymorphisms in ZFHX3 Are Associated with Atrial Fibrillation in a Chinese Han Population
}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}