{{Rsnum
|rsid=61753849
|Chromosome=12
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MYO1A
|position=57041441
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYO1A
}}{{omim
|id=601478
|rsnum=61753849
|variant=0004
}}{{ClinVar
|rsid=61753849
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=57435225
|CHROM=12
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000040002110100
|GENEINFO=MYO1A:4640
|GENE_NAME=MYO1A
|GENE_ID=4640
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.57435225C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601478.0004
|CLNSIG=5
|CLNCUI=C1842939
|CLNDBN=Deafness, autosomal dominant 48
|Disease=Deafness
|CLNACC=RCV000008626.1
|Tags=PM;S3D;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1842939:607841:90635
}}