{{Rsnum
|rsid=121912561
|Chromosome=6
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYO6
|position=75886881
|Gene_s=MYO6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600970
|rsnum=121912561
|variant=0006
}}{{ClinVar
|rsid=121912561
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=76596598
|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.76596598C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600970.0006
|CLNSIG=5
|CLNCUI=C1853441
|CLNDBN=Deafness, autosomal dominant 22
|Disease=Deafness
|CLNACC=RCV000009113.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1853441:606346:228012
}}