{{Rsnum
|rsid=281875232
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CYP26B1
|position=72135413
|Gene_s=CYP26B1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=2
|CLNACC=RCV000023401.1; RCV000059691.1
|CLNALLE=1
|CLNDBN=Radiohumeral fusions with other skeletal and craniofacial anomalies; not provided
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3280729:614416:293925
|CLNHGVS=NC_000002.11:g.72362542A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=605207.0002; VAR_067923
|Disease=Radiohumeral fusions with other skeletal and craniofacial anomalies; not provided
|FwdALT=C
|FwdREF=T
|REF=A
|RSPOS=72362542
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=281875232
|GENEINFO=CYP26B1:56603
|GENE_ID=56603
|GENE_NAME=CYP26B1
}}{{PMID Auto
|PMID=22019272
|Title=Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid.
|OA=1
}}