{{Rsnum
|rsid=104894651
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=USH1G
|position=74922931
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OTOP2,USH1G
}}{{omim
|id=607696
|rsnum=104894651
|variant=0001
}}{{ClinVar
|rsid=104894651
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=72919026
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=USH1G:124590; OTOP2:92736
|GENE_NAME=USH1G; OTOP2
|GENE_ID=124590; 92736
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.72919026A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607696.0001
|CLNSIG=5
|CLNCUI=C1847089
|CLNDBN=Usher syndrome, type 1G
|Disease=Usher syndrome
|CLNACC=RCV000003048.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1265:C1847089:606943:231169:886
}}