{{Rsnum
|rsid=121908073
|Gene=TMC1
|Chromosome=9
|position=72694578
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TMC1
}}{{omim
|id=606706
|rsnum=121908073
|variant=0002
}}{{ClinVar
|rsid=121908073
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=75309494
|CHROM=9
|GMAF=0.0005
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000040016110100
|GENEINFO=TMC1:117531
|GENE_NAME=TMC1
|GENE_ID=117531
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.75309494C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606706.0002
|CLNSIG=5
|CLNCUI=C1832978
|CLNDBN=Deafness, autosomal recessive 7; Hereditary hearing loss and deafness
|Disease=Deafness; Hereditary hearing loss and deafness
|CLNACC=RCV000004319.1; RCV000041123.1
|Tags=PM;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1434:C1832978:600974:90636; NBK1434:C0236038:95827002
|COMMON=0
}}