{{Rsnum
|rsid=111033214
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYO7A
|position=77189348
|Gene_s=MYO7A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033214
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=76900393
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|GENEINFO=MYO7A:4647
|GENE_NAME=MYO7A
|GENE_ID=4647
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.76900393G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000036112.1
|CLNDBN=Retinitis pigmentosa-deafness syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=C0271097:500004:231183:886:57838006
|Disease=Retinitis pigmentosa-deafness syndrome
}}{{PMID Auto
|PMID=10425080
|Title=Identification of three novel mutations in the MYO7A gene
}}

{{PMID Auto
|PMID=12112664
|Title=Mutations in myosin VIIA (MYO7A) and usherin (USH2A) in Spanish patients with Usher syndrome types I and II, respectively.
}}