{{Rsnum
|rsid=397514607
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=OTOG
|position=17612638
|Gene_s=OTOG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=11
|CLNACC=RCV000033039.1
|CLNALLE=1
|CLNDBN=Deafness, autosomal recessive 18b
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN161008:614945:90636
|CLNHGVS=NC_000011.9:g.17634185C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604487.0002
|Disease=Deafness
|FwdALT=T
|FwdREF=C
|GENEINFO=OTOG:340990
|GENE_ID=340990
|GENE_NAME=OTOG
|REF=C
|RSPOS=17634185
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514607
}}