{{Rsnum
|rsid=104893951
|Chromosome=6
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FOXC1
|position=1610780
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FOXC1
}}{{omim
|id=601090
|rsnum=104893951
|variant=0004
}}{{ClinVar
|rsid=104893951
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=1611015
|CHROM=6
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FOXC1:2296
|GENE_NAME=FOXC1
|GENE_ID=2296
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.1611015T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601090.0004
|CLNSIG=5
|CLNCUI=C2678503; C0344559
|CLNDBN=Axenfeld anomaly; Axenfeld-Rieger syndrome type 3; Irido-corneo-trabecular dysgenesis
|Disease=Axenfeld anomaly; Axenfeld-Rieger syndrome type 3; Irido-corneo-trabecular dysgenesis
|CLNACC=RCV000008970.2; RCV000008971.1; RCV000008972.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen; MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0266548; C2678503:602482:782; C0344559:604229:708:204153003
}}