{{Rsnum
|rsid=104893958
|Chromosome=6
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FOXC1
|position=1610823
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FOXC1
}}{{omim
|id=601090
|rsnum=104893958
|variant=0003
}}{{ClinVar
|rsid=104893958
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=1611058
|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.1611058C>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000008969.1
|CLNDBN=Axenfeld anomaly
|CLNDSDB=MedGen
|CLNDSDBID=C0266548
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601090.0003
|Disease=Axenfeld anomaly
}}