{{Rsnum
|rsid=28937591
|Gene=OTOF
|Chromosome=2
|position=26461756
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=G
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OTOF
}}[[deafness]]
{{omim
|desc=DEAFNESS, AUTOSOMAL RECESSIVE 9
|id=603681
|rsnum=28937591
|variant=0005
}}

{{ClinVar
|rsid=28937591
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=26684624
|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.26684624G>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1251; 603681.0005
|CLNSIG=5
|CLNCUI=C1832828; C1832828
|CLNDBN=Deafness, autosomal recessive 9
|Disease=Deafness
|CLNACC=RCV000006512.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1251:NBK1434:C1832828:601071:90636
}}

{{PMID Auto
|PMID=12114484
|Title=Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}