{{Rsnum
|rsid=121908076
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TMC1
|position=72792329
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TMC1
}}{{omim
|id=606706
|rsnum=121908076
|variant=0006
}}{{ClinVar
|rsid=121908076
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=75407245
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=TMC1:117531
|GENE_NAME=TMC1
|GENE_ID=117531
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.75407245T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606706.0006
|CLNSIG=5
|CLNCUI=C1832978
|CLNDBN=Deafness, autosomal recessive 7
|Disease=Deafness
|CLNACC=RCV000004323.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1832978:600974:90636
}}