{{Rsnum
|rsid=397514500
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=USH1C
|position=17531233
|Gene_s=USH1C
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=11
|CLNACC=RCV000032622.1
|CLNALLE=1
|CLNDBN=Usher syndrome, type 1C
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1265:C1848604:276904:231169:886
|CLNHGVS=NC_000011.9:g.17552780C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605242.0011
|Disease=Usher syndrome
|FwdALT=A
|FwdREF=G
|GENEINFO=USH1C:10083
|GENE_ID=10083
|GENE_NAME=USH1C
|REF=C
|RSPOS=17552780
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514500
}}