{{Rsnum
|rsid=3782889
|Gene=MYL2
|Chromosome=12
|position=110912851
|Orientation=minus
|GMAF=0.09826
|Gene_s=MYL2
|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 | 0.9 | 12.6 | 86.5
| HCB | 3.6 | 32.1 | 64.2
| JPT | 3.5 | 26.5 | 69.9
| YRI | 0.0 | 9.5 | 90.5
| ASW | 0.0 | 8.8 | 91.2
| CHB | 3.6 | 32.1 | 64.2
| CHD | 3.7 | 39.4 | 56.9
| GIH | 2.0 | 28.7 | 69.3
| LWK | 1.8 | 5.5 | 92.7
| MEX | 0.0 | 3.4 | 96.6
| MKK | 0.0 | 4.5 | 95.5
| TSI | 0.0 | 11.8 | 88.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=23364394
|Title=A genome-wide association study of a coronary artery disease risk variant
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}