Rsid Chr Position P value Ref Alt Gwas trait Gene symbol Variant type PMID
rs10114470 chr9 117547772 0.0000000000000542 T C Leprosy TNFSF15 UTR-3 20018961
rs10114470 chr9 117547772 0.0000000000482 T C Crohn's disease TNFSF15 UTR-3 23266558
rs10114470 chr9 117547772 0.00000408 T C Leprosy TNFSF15 UTR-3 pha002872
rs7853287 chr9 117549327 0.0000000003 G A IgA levels TNFSF15 UTR-3 24676358
rs10117785 chr9 117551603 0.00000000000251 T A Crohn's disease TNFSF15 UTR-3 16221758
rs3810936 chr9 117552885 0.0000000000389 T C Crohn's disease TNFSF15 cds-synon 16221758
rs3810936 chr9 117552885 0.000000000000001 T C Crohn's disease TNFSF15 cds-synon 21102463
rs4246905 chr9 117553249 0.00000302 T C Crohn's disease TNFSF15 intron 16221758
rs4246905 chr9 117553249 0.000000000006 T C Ulcerative colitis TNFSF15 intron 21297633
rs4246905 chr9 117553249 3e-32 T C Inflammatory bowel disease TNFSF15 intron 23128233
rs6478108 chr9 117558703 0.0000000000000562 C T Crohn's disease TNFSF15 intron 16221758
rs6478108 chr9 117558703 0.0000246 C T Multiple complex diseases TNFSF15 intron 17554300
rs6478108 chr9 117558703 3e-21 C T Leprosy TNFSF15 intron 20018961
rs6478108 chr9 117558703 0.00000000701 C T Leprosy TNFSF15 intron 22019778
rs6478108 chr9 117558703 0.00000000368 C T Primary biliary cirrhosis TNFSF15 intron 23000144
rs6478108 chr9 117558703 0.00000000000153 C T Crohn's disease TNFSF15 intron 23266558
rs6478108 chr9 117558703 0.000000411 C T Leprosy TNFSF15 intron pha002872
rs4372078 chr9 117563687 0.000000000646 T G Crohn's disease TNFSF15 intron 16221758
rs4263839 chr9 117566440 0.0000149 A G Multiple complex diseases TNFSF15 intron 17554300
rs4263839 chr9 117566440 0.0000000003 A G Crohn's disease TNFSF15 intron 18587394
rs4263839 chr9 117566440 0.0000000003 A G Asthma TNFSF15 intron 21150878
rs4263839 chr9 117566440 0.00000000026 A G Multiple sclerosis TNFSF15 intron 22190364
rs4979462 chr9 117567013 0.000000000000338 C T Crohn's disease TNFSF15 intron 16221758
rs4979462 chr9 117567013 0.00000000000003 C T Primary biliary cirrhosis TNFSF15 intron 23000144
rs6478109 chr9 117568766 0.0000000000117 A G Crohn's disease TNFSF15 nearGene-5 16221758
rs6478109 chr9 117568766 0.00000000367 A G Crohn's disease TNFSF15 nearGene-5 18587394
rs6478109 chr9 117568766 0.00000003 A G Inflammatory bowel disease TNFSF15 nearGene-5 18758464
rs6478109 chr9 117568766 0.00000000000684 A G Crohn's disease TNFSF15 nearGene-5 23266558
rs6478109 chr9 117568766 0.0000000912 A G Leprosy TNFSF15 nearGene-5 pha002872
rs7848647 chr9 117569046 0.0000000000443 T C Crohn's disease TNFSF15 nearGene-5 16221758