{{Rsnum
|rsid=104893739
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FOXL2
|position=138946137
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=C3orf72,FOXL2
}}{{omim
|id=605597
|rsnum=104893739
|variant=0013
}}{{ClinVar
|rsid=104893739
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=138664979
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FOXL2:668; C3orf72:401089
|GENE_NAME=FOXL2; C3orf72
|GENE_ID=668; 401089
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.138664979G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605597.0013
|CLNSIG=5
|CLNCUI=C0220663
|CLNDBN=Blepharophimosis, ptosis, and epicanthus inversus
|Disease=Blepharophimosis
|CLNACC=RCV000005141.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1441:C0220663:110100:126
}}