{{Rsnum
|rsid=80356602
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=OTOF
|position=26464868
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OTOF
}}{{omim
|id=603681
|rsnum=80356602
|variant=0008
}}{{ClinVar
|rsid=80356602
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=26687736
|CHROM=2
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=OTOF:9381
|GENE_NAME=OTOF
|GENE_ID=9381
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.26687736C>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1251; 603681.0008
|CLNSIG=5
|CLNCUI=C1832828
|CLNDBN=Auditory neuropathy, autosomal recessive, 1; Deafness, autosomal recessive 9
|Disease=Auditory neuropathy; Deafness
|CLNACC=RCV000006514.1; RCV000021068.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C1832829; NBK1251:NBK1434:C1832828:601071:90636
}}{{PMID Auto
|PMID=12525542
|Title=Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene.
|OA=1
}}