{{Rsnum
|rsid = 28934610
|Gene = MYO7A
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=11
|position=77156904
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYO7A
}}{{omim
|desc=USHER SYNDROME, TYPE IB
|id=276903
|rsnum=28934610
|variant=0004
}}

{{ClinVar
|rsid=28934610
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=76867950
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MYO7A:4647
|GENE_NAME=MYO7A
|GENE_ID=4647
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.76867950G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=276903.0004
|CLNSIG=5
|CLNCUI=C1848638
|CLNDBN=Usher syndrome, type 1B; Retinitis pigmentosa-deafness syndrome
|Disease=Usher syndrome; Retinitis pigmentosa-deafness syndrome
|CLNACC=RCV000012624.21; RCV000036232.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen; MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=C1848638; C0271097:500004:231183:886:57838006
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}