{{Rsnum
|rsid=41298133
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYO7A
|position=77156969
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYO7A
}}{{omim
|id=276903
|rsnum=41298133
|variant=0002
}}

{{ClinVar
|rsid=41298133
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=76868015
|CHROM=11
|dbSNPBuildID=127
|SSR=16
|SAO=1
|VP=0x050268000000000402110100
|GENEINFO=MYO7A:4647
|GENE_NAME=MYO7A
|GENE_ID=4647
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.76868015C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=276903.0002
|CLNSIG=5
|CLNCUI=C1848638
|CLNDBN=Usher syndrome, type 1B; Retinitis pigmentosa-deafness syndrome
|Disease=Usher syndrome; Retinitis pigmentosa-deafness syndrome
|CLNACC=RCV000012622.23; RCV000036246.1
|Tags=PM;PMC;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=MedGen; MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=C1848638; C0271097:500004:231183:886:57838006
}}

{{PMID Auto
|PMID=7870171
|Title=Defective myosin VIIA gene responsible for Usher syndrome type 1B.
}}

{{PMID Auto
|PMID=9002678
|Title=Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}