{{Rsnum
|rsid=17042171
|Chromosome=4
|position=110787131
|Orientation=plus
|GMAF=0.2759
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 1.8 | 19.5 | 78.8
| HCB | 20.4 | 52.6 | 27.0
| JPT | 23.9 | 46.0 | 30.1
| YRI | 7.5 | 39.5 | 53.1
| ASW | 1.8 | 50.9 | 47.4
| CHB | 20.4 | 52.6 | 27.0
| CHD | 30.3 | 45.9 | 23.9
| GIH | 3.0 | 21.8 | 75.2
| LWK | 2.7 | 32.7 | 64.5
| MEX | 3.4 | 43.1 | 53.4
| MKK | 5.1 | 26.9 | 67.9
| TSI | 2.0 | 30.4 | 67.6
| 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=A
|Pval=4E-63
|OR=1.65
|ORtxt=None
|OA=1
}}

{{omim
|id=611494
|rsnum=17042171
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs17042171
|overall_frequency_n=30
|overall_frequency_d=128
|overall_frequency=0.234375
|n_genomes=26
|n_genomes_annotated=0
|n_haplomes=30
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}