{{Rsnum
|rsid=7646881
|Chromosome=3
|position=158735490
|Orientation=plus
|GMAF=0.1575
|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 | 5.3 | 30.1 | 64.6
| HCB | 0.0 | 5.9 | 94.1
| JPT | 0.0 | 0.9 | 99.1
| YRI | 5.4 | 44.2 | 50.3
| ASW | 5.3 | 42.1 | 52.6
| CHB | 0.0 | 5.9 | 94.1
| CHD | 0.9 | 2.8 | 96.3
| GIH | 5.9 | 37.6 | 56.4
| LWK | 5.5 | 42.7 | 51.8
| MEX | 0.0 | 19.3 | 80.7
| MKK | 15.5 | 48.4 | 36.1
| TSI | 3.0 | 41.6 | 55.4
| 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=A
  |Pval=2E-6
  |OR=1.39
  |ORtxt=[1.224-1.581]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}