{{Rsnum
|rsid=121908932
|Chromosome=14
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=COCH
|position=30889763
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=COCH,RPS4XP13
}}{{omim
|id=603196
|rsnum=121908932
|variant=0007
}}{{ClinVar
|rsid=121908932
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=31358969
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=RP11-829H16.3:100506071; COCH:1690
|GENE_NAME=RP11-829H16.3; COCH
|GENE_ID=100506071; 1690
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000014.8:g.31358969G>A; NC_000014.8:g.31358969G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603196.0008; 603196.0007
|CLNSIG=5
|CLNCUI=C1832425
|CLNDBN=Deafness, autosomal dominant 9
|Disease=Deafness
|CLNACC=RCV000006994.1; RCV000006993.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1832425:601369:90635
}}