{{Rsnum
|rsid=121965079
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYO7A
|position=77156069
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYO7A
}}{{omim
|id=276903
|rsnum=121965079
|variant=0001
}}{{ClinVar
|rsid=121965079
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=76867115
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MYO7A:4647
|GENE_NAME=MYO7A
|GENE_ID=4647
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.76867115C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=276903.0001
|CLNSIG=5
|CLNCUI=C1848638
|CLNDBN=Usher syndrome, type 1B; Retinitis pigmentosa-deafness syndrome
|Disease=Usher syndrome; Retinitis pigmentosa-deafness syndrome
|CLNACC=RCV000012621.23; RCV000036148.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen; MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=C1848638; C0271097:500004:231183:886:57838006
}}