{{Rsnum
|rsid=2071731
|Gene=MYH9
|Chromosome=22
|position=36322813
|Orientation=plus
|GMAF=0.4233
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MYH9
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 12.4 | 48.7 | 38.9
| HCB | 59.1 | 36.5 | 4.4
| JPT | 67.0 | 28.6 | 4.5
| YRI | 1.4 | 37.4 | 61.2
| ASW | 8.8 | 35.1 | 56.1
| CHB | 59.1 | 36.5 | 4.4
| CHD | 75.2 | 21.1 | 3.7
| GIH | 30.7 | 48.5 | 20.8
| LWK | 5.5 | 36.4 | 58.2
| MEX | 13.8 | 34.5 | 51.7
| MKK | 3.2 | 25.6 | 71.2
| TSI | 8.8 | 46.1 | 45.1
| HapMapRevision=28
}}{{PMID Auto
|PMID=19320731
|Title=Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate
}}

{{PMID Auto
|PMID=18716610
|Title=Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate.
|OA=1
}}

{{PMID Auto
|PMID=20124285
|Title=Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.
|OA=1
}}

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