{{Rsnum
|rsid=2222823
|Gene=MYLK
|Chromosome=3
|position=123885940
|Orientation=minus
|GMAF=0.2117
|Gene_s=MYLK
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 90.8 | 9.2 | 0.0
| HCB | 46.7 | 40.0 | 13.3
| JPT | 45.5 | 50.0 | 4.5
| YRI | 49.2 | 39.7 | 11.1
| ASW | 0.0 | 0.0 | 0.0
| CHB | 46.7 | 40.0 | 13.3
| 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
|PMID=22621687
|Title=Heterozygote Genotypes at rs2222823 and rs2811712 SNP Loci are Associated with Cerebral Small Vessel Disease in Han Chinese Population
}}