{{Rsnum
|rsid=6499100
|Chromosome=16
|position=52797550
|Orientation=plus
|GMAF=0.4729
|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 | 14.3 | 49.1 | 36.6
| HCB | 59.6 | 34.6 | 5.9
| JPT | 47.8 | 38.9 | 13.3
| YRI | 4.8 | 23.1 | 72.1
| ASW | 1.8 | 46.4 | 51.8
| CHB | 59.6 | 34.6 | 5.9
| CHD | 64.2 | 29.4 | 6.4
| GIH | 25.7 | 52.5 | 21.8
| LWK | 5.5 | 50.0 | 44.5
| MEX | 50.0 | 39.7 | 10.3
| MKK | 2.6 | 28.8 | 68.6
| TSI | 23.5 | 39.2 | 37.3
| 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=A
  |Pval=1E-6
  |OR=1.26
  |ORtxt=[1.14-1.4]
  |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}}