{{Rsnum
|rsid=80356590
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=OTOF
|position=26479356
|Gene_s=OTOF
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356590
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=26702224
|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.26702224G>A
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=601071
|CLNDBN=Deafness, autosomal recessive 9; Hereditary hearing loss and deafness
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000021043.1; RCV000041481.1
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1251:NBK1434:C1832828:601071:90636; NBK1434:C0236038:95827002
|CLNSRC=GeneReviews
|CLNSRCID=NBK1251
|Disease=Deafness; Hereditary hearing loss and deafness
}}{{PMID Auto
|PMID=14635104
|Title=Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF).
}}