{{Rsnum
|rsid=111033283
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYO7A
|position=77156909
|Gene_s=MYO7A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033283
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=76867955
|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.76867955G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000036233.1
|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=9382091
|Title=Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.
|OA=1
}}

{{PMID Auto
|PMID=16470552
|Title=Mutation profile of the MYO7A gene in Spanish patients with Usher syndrome type I.
}}

{{PMID Auto
|PMID=18181211
|Title=Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
}}