{{Rsnum
|rsid=397517973
|Chromosome=1
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=USH2A
|position=215743314
|Gene_s=USH2A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000041696.1
|CLNALLE=1
|CLNDBN=Retinitis pigmentosa-deafness syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=C0271097:500004:ORPHA231183:ORPHA886:57838006
|CLNHGVS=NC_000001.11:g.215743314delG
|CLNSIG=5
|Disease=Retinitis pigmentosa-deafness syndrome
|FwdREF=C
|GENEINFO=USH2A:7399
|GENE_ID=7399
|GENE_NAME=USH2A
|REF=AG
|RSPOS=215743313
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSF;REF;ASP;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060001205000002110200
|WGT=1
|dbSNPBuildID=138
|rsid=397517973
|CLNORIGIN=1
|CLNSRC=ClinVar
|CLNSRCID=NM_206933.2:c.11411delC
}}