{{Rsnum
|rsid=55679042
|Gene=MYO1A
|Chromosome=12
|position=57043335
|Orientation=plus
|GMAF=0.002296
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MYO1A
}}{{omim
|id=601478
|rsnum=55679042
|variant=0003
}}{{ClinVar
|rsid=55679042
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=57437119
|CHROM=12
|GMAF=0.0023
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=MYO1A:4640
|GENE_NAME=MYO1A
|GENE_ID=4640
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.57437119C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601478.0003
|CLNSIG=5
|CLNCUI=C1842939
|CLNDBN=Deafness, autosomal dominant 48; AllHighlyPenetrant
|Disease=Deafness; AllHighlyPenetrant
|CLNACC=RCV000008625.1; RCV000038478.1
|Tags=PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9977; 0.002296
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1434:C1842939:607841:90635; CN169374
|COMMON=1
}}