{{Rsnum
|rsid=2251468
|Chromosome=12
|position=120967323
|Orientation=minus
|GMAF=0.3154
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 14.2 | 44.2 | 41.6
| HCB | 15.4 | 49.3 | 35.3
| JPT | 27.4 | 60.2 | 12.4
| YRI | 0.0 | 9.6 | 90.4
| ASW | 0.0 | 17.5 | 82.5
| CHB | 15.4 | 49.3 | 35.3
| CHD | 12.8 | 48.6 | 38.5
| GIH | 19.8 | 48.5 | 31.7
| LWK | 0.0 | 19.1 | 80.9
| MEX | 10.3 | 41.4 | 48.3
| MKK | 1.3 | 21.2 | 77.6
| TSI | 11.9 | 46.5 | 41.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23824729
  |Trait=Homocysteine levels
  |Title=Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.
  |RiskAllele=A
  |Pval=1E-12
  |OR=.05
  |ORtxt=[0.037-0.065] unit decrease
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}