{{Rsnum
|rsid=397515345
|Chromosome=17
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TCGGACGAGGACAGCGTCTC)
|geno3=(TCGGACGAGGACAGCGTCTC;TCGGACGAGGACAGCGTCTC)
|Gene=USH1G
|position=74919985
|Gene_s=USH1G
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=17
|CLNACC=RCV000003050.2
|CLNALLE=1
|CLNDBN=Usher syndrome, type 1G
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1265:C1847089:606943:231169:886
|CLNHGVS=NC_000017.10:g.72916080_72916099del20
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1265; 607696.0003
|Disease=Usher syndrome
|FwdREF=TCGGACGAGGACAGCGTCTC
|GENEINFO=USH1G:124590
|GENE_ID=124590
|GENE_NAME=USH1G
|REF=GGAGACGCTGTCCTCGTCCGA
|RSPOS=72916079
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=397515345
}}