{{Rsnum
|rsid=80356459
|Chromosome=14
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SIX1
|position=60648862
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SIX1
}}{{omim
|id=601205
|rsnum=80356459
|variant=0002
}}{{ClinVar
|rsid=80356459
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=61115580
|CHROM=14
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=SIX1:6495
|GENE_NAME=SIX1
|GENE_ID=6495
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.61115580G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1380; 601205.0002
|CLNSIG=5
|CLNCUI=C1842124; C1842124
|CLNDBN=Branchiootic syndrome 3
|Disease=Branchiootic syndrome 3
|CLNACC=RCV000008807.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1380:C1842124:608389
}}{{PMID Auto
|PMID=15141091
|Title=SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.
|OA=1
}}