{{Rsnum
|rsid=12134663
|Gene=LOC100506310
|Chromosome=1
|position=11778589
|Orientation=plus
|GMAF=0.1134
|Gene_s=LOC100506310
|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 | 63.5 | 31.7 | 4.8
| HCB | 83.3 | 16.7 | 0.0
| JPT | 86.4 | 13.6 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 83.3 | 16.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| 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=3E-21
  |OR=.10
  |ORtxt=[0.079-0.123] unit decrease
  }}