{{Rsnum
|rsid=80338828
|Chromosome=22
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYH9
|position=36305975
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYH9
}}{{omim
|id=160775
|rsnum=80338828
|variant=0008
}}{{ClinVar
|rsid=80338828
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=36702021
|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.36702021C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK2689; 160775.0008
|CLNSIG=5
|CLNCUI=C1863659
|CLNDBN=Deafness, autosomal dominant nonsyndromic sensorineural 17; MYH9 related disorders
|Disease=Deafness; MYH9 related disorders
|CLNACC=RCV000015130.24; RCV000032218.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen
|CLNDSDBID=NBK1434:C1863659:603622:90635; NBK2689:CN073381
}}{{PMID|9390828}} A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration.

{{PMID|11023810|OA=1
}} Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9.