{{Rsnum
|rsid=111033232
|Chromosome=11
|Orientation=plus
|geno1=(-;-)
|geno2=(-;CTT)
|geno3=(CTT;CTT)
|Gene=MYO7A
|position=77208459
|Gene_s=MYO7A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033232
|Reversed=0
|FwdREF=CTT
|FwdALT=
|REF=ACTT
|ALT=A
|RSPOS=76919497
|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.76919504_76919506delCTT
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000036213.1
|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=16679490
|Title=Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%.
|OA=1
}}