{{Rsnum
|rsid=397517925
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=USH1G
|position=74919463
|Gene_s=USH1G
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=17
|CLNACC=RCV000041415.1
|CLNALLE=1
|CLNDBN=Retinitis pigmentosa-deafness syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=C0271097:500004:231183:886:57838006
|CLNHGVS=NC_000017.10:g.72915558T>A
|CLNSIG=4
|Disease=Retinitis pigmentosa-deafness syndrome
|FwdALT=T
|FwdREF=A
|GENEINFO=USH1G:124590
|GENE_ID=124590
|GENE_NAME=USH1G
|REF=T
|RSPOS=72915558
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=397517925
}}