{{Rsnum
|rsid=80356605
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OTOF
|position=26460203
|Gene_s=OTOF
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356605
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=26683071
|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.26683071C>T
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=601071
|CLNDBN=Deafness, autosomal recessive 9; Auditory neuropathy, autosomal recessive, 1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000021073.1; RCV000033198.1
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1251:NBK1434:C1832828:601071:90636; C1832829
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1251; 603681.0012
|Disease=Deafness; Auditory neuropathy
}}{{PMID|12525542|OA=1
}} Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene.