{{Rsnum
|rsid=12186641
|Chromosome=5
|position=51868281
|Orientation=plus
|GMAF=0.04132
|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 | 87.6 | 9.7 | 2.7
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 95.9 | 4.1 | 0.0
| ASW | 93.0 | 7.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 95.0 | 4.0 | 1.0
| LWK | 85.5 | 14.5 | 0.0
| MEX | 84.5 | 15.5 | 0.0
| MKK | 83.2 | 16.1 | 0.6
| TSI | 85.3 | 13.7 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23708191
  |Trait=Congenital heart disease
  |Title=Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
  |RiskAllele=
  |Pval=7E-6
  |OR=1.68
  |ORtxt=[NR]
  |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 | Illumina Human 1M}}