{{Rsnum
|rsid=121909305
|Gene=MYO1A
|Chromosome=12
|position=57047675
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MYO1A
}}{{omim
|id=601478
|rsnum=121909305
|variant=0001
}}{{ClinVar
|rsid=121909305
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=57441459
|CHROM=12
|GMAF=0.0005
|dbSNPBuildID=133
|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.57441459G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601478.0001
|CLNSIG=5
|CLNCUI=C1842939
|CLNDBN=Deafness, autosomal dominant 48
|Disease=Deafness
|CLNACC=RCV000008623.1
|Tags=RV;PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1842939:607841:90635
|COMMON=0
}}