{{Rsnum
|rsid=79691946
|Gene=FOXC1
|Chromosome=6
|position=1611334
|Orientation=plus
|GMAF=0.03535
|Gene_s=FOXC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|ALT=T
|CAF=0.9646; 0.03535
|CHROM=6
|CLNACC=RCV000023070.1
|CLNALLE=1
|CLNDBN=Iridogoniodysgenesis type1
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1866560:601631
|CLNHGVS=NC_000006.11:g.1611569C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601090.0012
|COMMON=1
|Disease=Iridogoniodysgenesis type1
|FwdALT=T
|FwdREF=C
|GENEINFO=FOXC1:2296
|GENE_ID=2296
|GENE_NAME=FOXC1
|REF=C
|RSPOS=1611569
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000100516110100
|WGT=0
|dbSNPBuildID=131
|rsid=79691946
}}