{{Rsnum
|rsid=104893954
|Chromosome=6
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FOXC1
|position=1610706
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FOXC1
}}{{omim
|id=601090
|rsnum=104893954
|variant=0009
}}{{ClinVar
|rsid=104893954
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=1610941
|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.1610941C>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000008979.1
|CLNDBN=Axenfeld-rieger anomaly
|CLNDSDB=MedGen
|CLNDSDBID=C2676985
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601090.0009
|Disease=Axenfeld-rieger anomaly
}}