{{Rsnum
|rsid=41308425
|Chromosome=1
|position=215837990
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=USH2A
|Gene_s=USH2A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=1
|CLNACC=RCV000041950.1
|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.215837990C>G
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=ClinVar
|CLNSRCID=NM_206933.2:c.9371+1G>C
|Disease=Retinitis pigmentosa-deafness syndrome
|FwdALT=G
|FwdREF=C
|GENEINFO=USH2A:7399
|GENE_ID=7399
|GENE_NAME=USH2A
|REF=C
|RSPOS=215837990
|Reversed=0
|SAO=0
|SSR=0
|Tags=DSS;ASP;HD;OTHERKG
|VC=SNV
|VP=0x050000100005000402000100
|WGT=1
|dbSNPBuildID=127
|rsid=41308425
}}

{{on chip | HumanOmni1Quad}}