{{Rsnum
|rsid=820336
|Gene=MYLK
|Chromosome=3
|position=123696934
|Orientation=minus
|GMAF=0.3903
|Gene_s=MYLK
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 65.2 | 31.2 | 3.6
| HCB | 0.7 | 8.0 | 91.2
| JPT | 0.0 | 2.7 | 97.3
| YRI | 0.0 | 8.2 | 91.8
| ASW | 5.3 | 31.6 | 63.2
| CHB | 0.7 | 8.0 | 91.2
| CHD | 0.0 | 12.8 | 87.2
| GIH | 32.7 | 45.5 | 21.8
| LWK | 0.0 | 17.3 | 82.7
| MEX | 17.2 | 44.8 | 37.9
| MKK | 3.2 | 40.3 | 56.5
| TSI | 66.7 | 31.4 | 2.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=22015949
|Title=An intronic MYLK variant associated with inflammatory lung disease regulates promoter activity of the smooth muscle myosin light chain kinase isoform
}}

{{PMID|20081554}} Genetic variation in MYLK and lung injury in children and adults with community-acquired pneumonia.

{{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}}