Variant: rs1050152 

    present in Gene: SLC22A4;MIR3936HG
    present in Chromosome: 5
    Position on Chromosome: 132340627
    Alleles of this Variant: C/T

rs1050152 in SLC22A4;MIR3936HG 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.

rs1050152 in SLC22A4;MIR3936HG gene and Nasal Polyps PMID 30643255 2019 A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis.