{{Rsnum
|rsid=111033178
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYO7A
|position=77190108
|Gene_s=MYO7A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033178
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=76901153
|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.76901153G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000036122.1
|CLNDBN=Retinitis pigmentosa-deafness syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=C0271097:500004:231183:886:57838006
|Disease=Retinitis pigmentosa-deafness syndrome
}}{{PMID|10094549}} Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneity.

{{PMID|10930322}} Evaluation of the myosin VIIA gene and visual function in patients with Usher syndrome type I.

{{PMID|17361009|OA=1
}} MYO7A mutation screening in Usher syndrome type I patients from diverse origins.