{{Rsnum
|rsid=121908072
|Chromosome=9
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TMC1
|position=72816161
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TMC1
}}{{omim
|id=606706
|rsnum=121908072
|variant=0001
}}
{{omim
|id=606706
|rsnum=121908072
|variant=0004
}}{{ClinVar
|rsid=121908072
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=75431077
|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; 2
|CLNHGVS=NC_000009.11:g.75431077G>A; NC_000009.11:g.75431077G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606706.0001; 606706.0004
|CLNSIG=5
|CLNCUI=C1847626
|CLNDBN=Deafness, autosomal dominant 36
|Disease=Deafness
|CLNACC=RCV000004318.1; RCV000004321.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1847626:606705:90635
}}