{{Rsnum
|rsid=387906699
|Chromosome=11
|position=77174831
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYO7A
|Gene_s=MYO7A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=11
|CLNACC=RCV000022816.13
|CLNALLE=1
|CLNDBN=Deafness, autosomal dominant 11
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1832475:601317:90635
|CLNHGVS=NC_000011.9:g.76885877G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=276903.0020
|Disease=Deafness
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=76885877
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906699
|GENEINFO=MYO7A:4647
|GENE_ID=4647
|GENE_NAME=MYO7A
}}