{{Rsnum
|rsid=111033286
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYO7A
|position=77162146
|Gene_s=MYO7A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033286
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=76873192
|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.76873192C>T
|CLNORIGIN=1
|CLNSIG=4
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000036048.1
|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=10930322
|Title=Evaluation of the myosin VIIA gene and visual function in patients with Usher syndrome type I.
}}

{{PMID Auto
|PMID=16963483
|Title=Development of a genotyping microarray for Usher syndrome.
|OA=1
}}

{{PMID Auto
|PMID=17407589
|Title=Deafblindness in French Canadians from Quebec: a predominant founder mutation in the USH1C gene provides the first genetic link with the Acadian population.
|OA=1
}}