{{Rsnum
|rsid=2388896
|Chromosome=10
|position=8954224
|Orientation=plus
|GMAF=0.32
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 12.4 | 45.1 | 42.5
| HCB | 2.2 | 34.6 | 63.2
| JPT | 7.1 | 43.4 | 49.6
| YRI | 13.6 | 46.3 | 40.1
| ASW | 14.0 | 42.1 | 43.9
| CHB | 2.2 | 34.6 | 63.2
| CHD | 1.9 | 25.9 | 72.2
| GIH | 14.0 | 44.0 | 42.0
| LWK | 18.2 | 46.4 | 35.5
| MEX | 3.4 | 24.1 | 72.4
| MKK | 16.7 | 52.6 | 30.8
| TSI | 15.7 | 48.0 | 36.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23297363
  |Trait=Tetralogy of Fallot
  |Title=Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot.
  |RiskAllele=G
  |Pval=9E-8
  |OR=1.28
  |ORtxt=[1.15-1.43]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}