Variant: rs4263839 

    present in Gene: TNFSF15
    present in Chromosome: 9
    Position on Chromosome: 114804160
    Alleles of this Variant: A/G

rs4263839 in TNFSF15 gene and Asthma PMID 21150878 2011 Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia.

rs4263839 in TNFSF15 gene and Crohn Disease PMID 18587394 2008 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.

rs4263839 in TNFSF15 gene and Multiple Sclerosis PMID 22190364 2011 Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.