{{Rsnum
|rsid=2474937
|Chromosome=1
|position=118360355
|Orientation=minus
|GMAF=0.2107
|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 | 2.7 | 32.7 | 64.6
| HCB | 0.0 | 18.2 | 81.8
| JPT | 0.0 | 8.0 | 92.0
| YRI | 8.2 | 49.7 | 42.2
| ASW | 7.0 | 49.1 | 43.9
| CHB | 0.0 | 18.2 | 81.8
| CHD | 0.0 | 13.8 | 86.2
| GIH | 5.9 | 47.5 | 46.5
| LWK | 11.8 | 45.5 | 42.7
| MEX | 1.7 | 39.7 | 58.6
| MKK | 5.8 | 39.1 | 55.1
| TSI | 5.9 | 32.4 | 61.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23708190
  |Trait=Congenital heart malformation
  |Title=A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations.
  |RiskAllele=C
  |Pval=8E-10
  |OR=1.40
  |ORtxt=[1.26-1.56]
  }}

{{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}}