Variant: rs281875231 

    present in Gene: CYP26B1
    present in Chromosome: 2
    Position on Chromosome: 72133081
    Alleles of this Variant: C/A;T

rs281875231 in CYP26B1 gene and RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES PMID 22019272 2011 Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid.