{{Rsnum
|rsid=121912560
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYO6
|position=75841299
|Gene_s=MYO6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600970
|rsnum=121912560
|variant=0005
}}{{ClinVar
|rsid=121912560
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=76551016
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MYO6:4646
|GENE_NAME=MYO6
|GENE_ID=4646
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.76551016A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600970.0005
|CLNSIG=5
|CLNCUI=C1853442
|CLNDBN=Sensorineural deafness with hypertrophic cardiomyopathy
|Disease=Sensorineural deafness with hypertrophic cardiomyopathy
|CLNACC=RCV000009112.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C3501265
}}