{{Rsnum
|rsid=80356460
|Chromosome=14
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GAG)
|geno3=(GAG;GAG)
|Gene=SIX1
|position=60648791
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SIX1
}}{{omim
|id=601205
|rsnum=80356460
|variant=0003
}}{{ClinVar
|rsid=80356460
|Reversed=1
|FwdREF=GAG
|FwdALT=
|REF=TCTC
|ALT=T
|RSPOS=61115508
|CHROM=14
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=SIX1:6495
|GENE_NAME=SIX1
|GENE_ID=6495
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.61115509_61115511delCTC
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1380; 601205.0003
|CLNSIG=5
|CLNCUI=C1854594; C1842124
|CLNDBN=Deafness, autosomal dominant 23; Branchiootic syndrome 3
|Disease=Deafness; Branchiootic syndrome 3
|CLNACC=RCV000008808.1; RCV000020636.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1434:C1854594:605192:90635; NBK1380:C1842124:608389
}}{{PMID Auto
|PMID=10777717
|Title=A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred.
|OA=1
}}

{{PMID Auto
|PMID=15141091
|Title=SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.
|OA=1
}}