{{Rsnum
|rsid=11089788
|Gene=MYH9
|Chromosome=22
|position=36355056
|Orientation=plus
|GMAF=0.3549
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=MYH9
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 25.7 | 50.4 | 23.9
| HCB | 0.7 | 12.4 | 86.9
| JPT | 0.0 | 9.7 | 90.3
| YRI | 17.8 | 50.0 | 32.2
| ASW | 17.5 | 50.9 | 31.6
| CHB | 0.7 | 12.4 | 86.9
| CHD | 0.9 | 7.3 | 91.7
| GIH | 3.0 | 33.7 | 63.4
| LWK | 17.4 | 43.1 | 39.4
| MEX | 19.0 | 50.0 | 31.0
| MKK | 9.6 | 42.9 | 47.4
| TSI | 27.5 | 47.1 | 25.5
| HapMapRevision=28
}}{{PMID Auto
|PMID=19387472
|Title=Genome-wide linkage analysis of serum creatinine in three isolated European populations
}}

{{PMID Auto
|PMID=21245129
|Title=Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with the progression of IgA nephropathy in Chinese
}}

{{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
}}

{{PMID Auto
|PMID=23516419
|Title=Epistatic Role of the MYH9/APOL1 Region on Familial Hematuria Genes
|OA=1
}}

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