{{Rsnum
|rsid=35689081
|Gene=MYO7A
|Chromosome=11
|position=77142783
|Orientation=plus
|GMAF=0.01469
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MYO7A
}}{{omim
|id=276903
|rsnum=35689081
|variant=0013
}}

{{ClinVar
|rsid=35689081
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=76853829
|CHROM=11
|GMAF=0.0147
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050160000000150516110100
|GENEINFO=MYO7A:4647
|GENE_NAME=MYO7A
|GENE_ID=4647
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.76853829C>A; NC_000011.9:g.76853829C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=276903.0013
|CLNSIG=5
|CLNCUI=C1848638
|CLNDBN=Usher syndrome, type 1B; AllHighlyPenetrant
|Disease=Usher syndrome; AllHighlyPenetrant
|CLNACC=RCV000012634.23; RCV000036252.1
|Tags=PM;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9853; 0.01469
|CLNDSDB=MedGen
|CLNDSDBID=C1848638; CN169374
|COMMON=1
}}

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