{{Rsnum
|rsid=80358194
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=FOXE3
|position=47417035
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FOXE3
}}{{omim
|id=601094
|rsnum=80358194
|variant=0002
}}{{ClinVar
|rsid=80358194
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=47417035
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000605000002110100
|GENEINFO=FOXE3:2301
|GENE_NAME=FOXE3
|GENE_ID=2301
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.47417035C>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_012186.2:c.720C>A; 601094.0002
|CLNSIG=5
|CLNCUI=C1853230
|CLNDBN=Aphakia, congenital primary
|Disease=Aphakia
|CLNACC=RCV000008963.1
|Tags=PM;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1853230:610256:ORPHA83461
}}