{{Rsnum
|rsid=111033192
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYO7A
|position=77207370
|Gene_s=MYO7A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033192
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=76918415
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002100100
|GENEINFO=MYO7A:4647
|GENE_NAME=MYO7A
|GENE_ID=4647
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.76918415G>A; NC_000011.9:g.76918415G>T
|CLNORIGIN=1
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000036204.1; RCV000036205.1
|Tags=PM;S3D;OTHERKG;LSD
|CLNDBN=AllHighlyPenetrant; Retinitis pigmentosa-deafness syndrome
|CLNDSDB=MedGen; MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=CN169374; C0271097:500004:231183:886:57838006
|Disease=AllHighlyPenetrant; Retinitis pigmentosa-deafness syndrome
}}