{{Rsnum
|rsid=5757949
|Gene=MKL1
|Chromosome=22
|position=40424147
|Orientation=plus
|GMAF=0.2388
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MKL1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 9.7 | 38.9 | 51.3
| HCB | 16.8 | 49.6 | 33.6
| JPT | 8.0 | 40.7 | 51.3
| YRI | 0.0 | 0.0 | 100.0
| ASW | 1.8 | 12.3 | 86.0
| CHB | 16.8 | 49.6 | 33.6
| CHD | 15.6 | 55.0 | 29.4
| GIH | 1.0 | 28.7 | 70.3
| LWK | 0.0 | 1.8 | 98.2
| MEX | 1.7 | 27.6 | 70.7
| MKK | 1.3 | 14.1 | 84.6
| TSI | 11.8 | 45.1 | 43.1
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19570815
|Trait=Height
|Title=A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation
|RiskAllele=T
|Pval=0.000004
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs5757949
|overall_frequency_n=26
|overall_frequency_d=128
|overall_frequency=0.203125
|n_genomes=18
|n_genomes_annotated=0
|n_haplomes=20
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}