{{Rsnum
|rsid=80338827
|Chromosome=22
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYH9
|position=36305984
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYH9
}}{{omim
|id=160775
|rsnum=80338827
|variant=0009
}}{{ClinVar
|rsid=80338827
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=36702030
|CHROM=22
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=MYH9:4627
|GENE_NAME=MYH9
|GENE_ID=4627
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.36702030C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK2689; 160775.0009
|CLNSIG=5
|CLNCUI=C0403445; C0398641
|CLNDBN=Fechtner syndrome; Epstein syndrome; MYH9 related disorders
|Disease=Fechtner syndrome; Epstein syndrome; MYH9 related disorders
|CLNACC=RCV000015132.24; RCV000015133.24; RCV000032217.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT; GeneReviews:MedGen
|CLNDSDBID=NBK2689:C0403445:153640:236422008; NBK2689:C0398641:153650:234485006; NBK2689:CN073381
}}{{PMID|11590545|OA=1
}} Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.

{{PMID|11935325}} Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene.