{{Rsnum
|rsid=104894110
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FOXE1
|position=97854108
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FOXE1,RP11-23B15.1
}}{{omim
|id=602617
|rsnum=104894110
|variant=0001
}}{{ClinVar
|rsid=104894110
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=100616390
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FOXE1:2304
|GENE_NAME=FOXE1
|GENE_ID=2304
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.100616390C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602617.0001
|CLNSIG=5
|CLNCUI=C1855794
|CLNDBN=Bamforth syndrome
|Disease=Bamforth syndrome
|CLNACC=RCV000007402.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1855794:241850:1226
}}