{{Rsnum
|rsid=104894478
|Chromosome=14
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SIX1
|position=60648804
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SIX1
}}{{omim
|id=601205
|rsnum=104894478
|variant=0001
}}{{ClinVar
|rsid=104894478
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=61115522
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SIX1:6495
|GENE_NAME=SIX1
|GENE_ID=6495
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.61115522T>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1380; 601205.0001
|CLNSIG=5
|CLNCUI=C1842124
|CLNDBN=Branchiootic syndrome 3; Melnick-Fraser syndrome
|Disease=Branchiootic syndrome 3; Melnick-Fraser syndrome
|CLNACC=RCV000008806.1; RCV000055925.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1380:C1842124:608389; NBK1380:C0265234:113650:107:290006
}}