{{Rsnum
|rsid=121965082
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYO7A
|position=77166162
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYO7A
}}{{omim
|id=276903
|rsnum=121965082
|variant=0010
}}{{ClinVar
|rsid=121965082
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=76877208
|CHROM=11
|dbSNPBuildID=133
|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.76877208G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=276903.0010
|CLNSIG=5
|CLNCUI=C1838701; C1848638
|CLNDBN=Deafness, autosomal recessive 2; Usher syndrome, type 1B
|Disease=Deafness; Usher syndrome
|CLNACC=RCV000012630.13; RCV000012631.21
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=C1838701:600060:90636; C1848638
}}