{{Rsnum
|rsid=80338834
|Chromosome=22
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYH9
|position=36284474
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYH9
}}{{omim
|id=160775
|rsnum=80338834
|variant=0002
}}{{ClinVar
|rsid=80338834
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=36680520
|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.36680520C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK2689; 160775.0002
|CLNSIG=5
|CLNCUI=C0340978; C0403445
|CLNDBN=May-Hegglin anomaly; Fechtner syndrome; MYH9 related disorders
|Disease=May-Hegglin anomaly; Fechtner syndrome; MYH9 related disorders
|CLNACC=RCV000015119.24; RCV000015120.24; RCV000032226.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen:OMIM:SNOMED_CT; GeneReviews:MedGen
|CLNDSDBID=NBK2689:C0340978:155100; NBK2689:C0403445:153640:236422008; NBK2689:CN073381
}}{{PMID Auto
|PMID=10973259
|Title=Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.
}}

{{PMID Auto
|PMID=10973260
|Title=Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly.
}}