{{Rsnum
|rsid=121909337
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FOXF1
|position=86513083
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FOXF1
}}{{omim
|id=601089
|rsnum=121909337
|variant=0002
}}{{ClinVar
|rsid=121909337
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=86546689
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FOXF1:2294
|GENE_NAME=FOXF1
|GENE_ID=2294
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.86546689T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601089.0002
|CLNSIG=5
|CLNCUI=C0031190
|CLNDBN=Alveolar capillary dysplasia with misalignment of pulmonary veins
|Disease=Alveolar capillary dysplasia with misalignment of pulmonary veins
|CLNACC=RCV000008984.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0031190:265380:210122
}}