{{Rsnum
|rsid=397517988
|Chromosome=1
|Orientation=minus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=USH2A
|position=215671073
|Gene_s=USH2A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=CT
|CHROM=1
|CLNACC=RCV000041749.1
|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.215671074dupT
|CLNSIG=5
|Disease=Retinitis pigmentosa-deafness syndrome
|FwdALT=A
|GENEINFO=USH2A:7399
|GENE_ID=7399
|GENE_NAME=USH2A
|REF=C
|RSPOS=215671073
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSF;REF;ASP;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060001205000002110200
|WGT=1
|dbSNPBuildID=138
|rsid=397517988
|CLNORIGIN=1
|CLNSRC=ClinVar
|CLNSRCID=NM_206933.2:c.14031_14032insA
}}