{{Rsnum
|rsid=119103280
|Gene=MYH14
|Chromosome=19
|position=50244277
|Orientation=plus
|GMAF=0.002755
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=MYH14
}}{{omim
|id=608568
|rsnum=119103280
|variant=0004
}}{{ClinVar
|rsid=119103280
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=50747534
|CHROM=19
|GMAF=0.0027
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=MYH14:79784
|GENE_NAME=MYH14
|GENE_ID=79784
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.50747534G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608568.0004
|CLNSIG=5
|CLNCUI=C1833503
|CLNDBN=Deafness, autosomal dominant 4; AllHighlyPenetrant
|Disease=Deafness; AllHighlyPenetrant
|CLNACC=RCV000002283.1; RCV000037022.1
|Tags=PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9972; 0.002755
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1434:C1833503:600652:90635; CN169374
|COMMON=1
}}