{{Rsnum
|rsid=28940306
|Gene=MYH14
|Chromosome=19
|position=50271424
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYH14
}}[[deafness]]
{{omim
|desc=DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 4
|id=608568
|rsnum=28940306
|variant=0002
}}{{ClinVar
|rsid=28940306
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=50774681
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MYH14:79784
|GENE_NAME=MYH14
|GENE_ID=79784
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.50774681C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608568.0002
|CLNSIG=5
|CLNCUI=C1833503
|CLNDBN=Deafness, autosomal dominant 4
|Disease=Deafness
|CLNACC=RCV000002281.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1833503:600652:90635
}}