{{Rsnum
|rsid=80356463
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SIX5
|position=45766866
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SIX5
}}{{omim
|id=600963
|rsnum=80356463
|variant=0003
}}{{ClinVar
|rsid=80356463
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=46270124
|CHROM=19
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=SIX5:147912
|GENE_NAME=SIX5
|GENE_ID=147912
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.46270124C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1380; 600963.0003
|CLNSIG=5
|CLNCUI=C1970479; C1970479
|CLNDBN=Branchiootorenal syndrome 2
|Disease=Branchiootorenal syndrome 2
|CLNACC=RCV000009131.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1380:C1970479:610896:107
}}{{PMID Auto
|PMID=17357085
|Title=Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome.
|OA=1
}}