{{Rsnum
|rsid=3853445
|Chromosome=4
|position=110840331
|Orientation=plus
|GMAF=0.2456
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.0 | 36.3 | 55.8
| HCB | 7.4 | 49.3 | 43.4
| JPT | 15.9 | 42.5 | 41.6
| YRI | 0.7 | 14.3 | 85.0
| ASW | 0.0 | 12.3 | 87.7
| CHB | 7.4 | 49.3 | 43.4
| CHD | 15.6 | 45.0 | 39.4
| GIH | 14.9 | 39.6 | 45.5
| LWK | 3.6 | 14.5 | 81.8
| MEX | 19.0 | 51.7 | 29.3
| MKK | 2.6 | 35.3 | 62.2
| TSI | 6.9 | 32.4 | 60.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=20733104
|Title=Independent Susceptibility Markers for Atrial Fibrillation on Chromosome 4q25
|OA=1
}}

{{PMID Auto
|PMID=21760908
|Title=Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}