{{Rsnum
|rsid=41282932
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=USH1C
|position=17509546
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=USH1C
}}{{omim
|id=605242
|rsnum=41282932
|variant=0009
}}

{{ClinVar
|rsid=41282932
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=17531093
|CHROM=11
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050068000000040002110100
|GENEINFO=USH1C:10083
|GENE_NAME=USH1C
|GENE_ID=10083
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.17531093G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605242.0009
|CLNSIG=5
|CLNCUI=C1865870
|CLNDBN=Deafness, autosomal recessive 18; AllHighlyPenetrant
|Disease=Deafness; AllHighlyPenetrant
|CLNACC=RCV000005455.1; RCV000041259.1
|Tags=PM;PMC;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1434:C1865870:602092:90636; CN169374
}}

{{PMID Auto
|PMID=12136232
|Title=Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness.
}}

{{PMID Auto
|PMID=16963483
|Title=Development of a genotyping microarray for Usher syndrome.
|OA=1
}}

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