{{Rsnum
|rsid=7616330
|Gene=FOXP1
|Chromosome=3
|position=71066600
|Orientation=plus
|GMAF=0.286
|Gene_s=FOXP1
|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 | 29.2 | 69.0
| HCB | 29.2 | 46.7 | 24.1
| JPT | 37.2 | 57.5 | 5.3
| YRI | 2.0 | 32.7 | 65.3
| ASW | 0.0 | 35.1 | 64.9
| CHB | 29.2 | 46.7 | 24.1
| CHD | 31.2 | 44.0 | 24.8
| GIH | 11.9 | 43.6 | 44.6
| LWK | 6.4 | 30.0 | 63.6
| MEX | 3.4 | 29.3 | 67.2
| MKK | 1.3 | 23.7 | 75.0
| TSI | 1.0 | 18.6 | 80.4
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23166209
  |Trait=QT interval
  |Title=Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans.
  |RiskAllele=A
  |Pval=6E-6
  |OR=1.72
  |ORtxt=[0.99-2.45] unit increase
  |OA=1
}}

{{on chip | Illumina Human 1M}}