Variant: rs272888 

    present in Gene: MIR3936HG;SLC22A4
    present in Chromosome: 5
    Position on Chromosome: 132329730
    Alleles of this Variant: T/C

rs272888 in MIR3936HG;SLC22A4 gene and Crohn Disease PMID 17804789 2007 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.