{{Rsnum
|rsid=111033219
|Chromosome=11
|Orientation=plus
|geno1=(-;-)
|geno2=(-;GCA)
|geno3=(GCA;GCA)
|Gene=MYO7A
|position=77162179
|Gene_s=MYO7A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033219
|Reversed=0
|FwdALT=GCA
|REF=G
|ALT=GGCA
|RSPOS=76873222
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050068000000000002100200
|GENEINFO=MYO7A:4647
|GENE_NAME=MYO7A
|GENE_ID=4647
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.76873225_76873226insGCA
|CLNORIGIN=1
|CLNSIG=4
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000036049.1
|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=8900236
|Title=Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.
|OA=1
}}