{{Rsnum
|rsid=281865415
|Chromosome=11
|position=121166652
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TECTA
|Gene_s=TECTA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=T
|CHROM=11
|CLNACC=RCV000007428.1
|CLNALLE=1
|CLNDBN=Deafness, autosomal dominant 12
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1832187:601543:90635
|CLNHGVS=NC_000011.9:g.121037361C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602574.0001
|Disease=Deafness
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=121037361
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=281865415
|GENEINFO=TECTA:7007
|GENE_ID=7007
|GENE_NAME=TECTA
}}