{{Rsnum
|rsid=80356585
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=OTOF
|position=26482516
|Gene_s=OTOF
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356585
|Reversed=1
|FwdREF=C
|FwdALT=A,G,T
|REF=G
|ALT=A,C,T
|RSPOS=26705384
|CHROM=2
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110104
|GENEINFO=OTOF:9381
|GENE_NAME=OTOF
|GENE_ID=9381
|WGT=0
|VC=SNV
|CLNALLE=2; 3
|CLNHGVS=NC_000002.11:g.26705384G>C; NC_000002.11:g.26705384G>T
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=601071
|CLNDBN=AllHighlyPenetrant; Deafness, autosomal recessive 9
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM;NOV
|CLNACC=RCV000041460.1; RCV000021034.1
|CLNDSDB=MedGen; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=CN169374; NBK1251:NBK1434:C1832828:601071:90636
|CLNSRC=GeneReviews
|CLNSRCID=NBK1251
|Disease=AllHighlyPenetrant; Deafness
}}{{PMID Auto
|PMID=12127154
|Title=Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafness.
}}