{{Rsnum
|rsid=121908933
|Chromosome=14
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=COCH
|position=30889763
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=COCH,RPS4XP13
|Status=Merged
|Merged=121908932
}}{{omim
|id=603196
|rsnum=121908933
|variant=0008
}}{{ClinVar
|rsid=121908933
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=31358969
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=050060000a15000002110100
|GENEINFO=COCH:1690; LOC100506071:100506071
|GENE_NAME=COCH; LOC100506071
|GENE_ID=1690; 100506071
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.31358969G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603196.0008
|CLNSIG=5
|CLNCUI=C1832425
|CLNDBN=Deafness, autosomal dominant 9
|Disease=Deafness
|CLNACC=SCV000027190.1
|Tags=PM;NSM;REF;OTH;ASP;OTHERKG;LSD;OM
}}