{{Rsnum
|rsid=111033364
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=USH2A
|position=215728232
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=USH2A
}}{{omim
|id=608400
|rsnum=111033364
|variant=0007
}}{{ClinVar
|rsid=111033364
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=215728232
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050068000605000002110100
|GENEINFO=USH2A:7399
|GENE_NAME=USH2A
|GENE_ID=7399
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.215728232C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_206933.2:c.11864G>A; 608400.0007
|CLNSIG=5
|CLNCUI=C1848634
|CLNDBN=Usher syndrome, type 2A; Retinitis pigmentosa-deafness syndrome
|Disease=Usher syndrome; Retinitis pigmentosa-deafness syndrome
|CLNACC=RCV000002451.1; RCV000041705.1
|Tags=RV;PM;PMC;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet; MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1341:C1848634:276901:ORPHA231178:ORPHA886; C0271097:500004:ORPHA231183:ORPHA886:57838006
}}{{PMID Auto
|PMID=15015129
|Title=Identification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type II.
|OA=1
}}

{{PMID Auto
|PMID=16963483
|Title=Development of a genotyping microarray for Usher syndrome.
|OA=1
}}