{{Rsnum
|rsid=80356600
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=OTOF
|position=26466723
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OTOF
}}{{omim
|id=603681
|rsnum=80356600
|variant=0001
}}{{ClinVar
|rsid=80356600
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=26689591
|CHROM=2
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=OTOF:9381
|GENE_NAME=OTOF
|GENE_ID=9381
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.26689591A>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1251; 603681.0001
|CLNSIG=5
|CLNCUI=C1832828
|CLNDBN=Deafness, autosomal recessive 9
|Disease=Deafness
|CLNACC=RCV000006507.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1251:NBK1434:C1832828:601071:90636
}}{{PMID Auto
|PMID=10903124
|Title=OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9.
|OA=1
}}