{{Rsnum
|rsid=80356597
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=OTOF
|position=26473296
|Gene_s=OTOF
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356597
|Reversed=1
|FwdREF=A
|FwdALT=C
|REF=T
|ALT=G
|RSPOS=26696164
|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.26696164T>G
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=601071
|CLNDBN=Deafness, autosomal recessive 9
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000021058.1
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1251:NBK1434:C1832828:601071:90636
|CLNSRC=GeneReviews
|CLNSRCID=NBK1251
|Disease=Deafness
}}{{PMID Auto
|PMID=12525542
|Title=Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene.
|OA=1
}}