{{Rsnum
|rsid=28938175
|Gene=COCH
|Chromosome=14
|position=30877640
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=COCH,RPS4XP13
}}[[deafness]]
{{omim
|desc=DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 9
|id=603196
|rsnum=28938175
|variant=0004
}}{{ClinVar
|rsid=28938175
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=31346846
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RP11-829H16.3:100506071; COCH:1690
|GENE_NAME=RP11-829H16.3; COCH
|GENE_ID=100506071; 1690
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.31346846C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603196.0004
|CLNSIG=5
|CLNCUI=C1832425
|CLNDBN=Deafness, autosomal dominant 9; Hereditary hearing loss and deafness
|Disease=Deafness; Hereditary hearing loss and deafness
|CLNACC=RCV000006990.2; RCV000037875.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1434:C1832425:601369:90635; NBK1434:C0236038:95827002
}}