{{Rsnum
|rsid=121908370
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=USH1C
|position=17533268
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=USH1C
}}{{omim
|id=605242
|rsnum=121908370
|variant=0007
}}{{ClinVar
|rsid=121908370
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=17554815
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=USH1C:10083
|GENE_NAME=USH1C
|GENE_ID=10083
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.17554815G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605242.0007
|CLNSIG=5
|CLNCUI=C1848604
|CLNDBN=Usher syndrome, type 1C
|Disease=Usher syndrome
|CLNACC=RCV000005453.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1265:C1848604:276904:231169:886
}}