Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4263839
rs4263839
TNFSF15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.830 GeneticVariation GWASCAT Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394

2008
dbSNP: rs6478109
rs6478109
TNFSF15
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 GeneticVariation GWASCAT Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. 18758464

2008
dbSNP: rs6478108
rs6478108
TNFSF15
CUI: C0023343
Disease: Leprosy
Leprosy 		A 0.810 GeneticVariation GWASCAT Genomewide association study of leprosy. 20018961

2009
dbSNP: rs3810936
rs3810936
TNFSF15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		C 0.850 GeneticVariation GWASCAT Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463

2010
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		C 0.800 GeneticVariation GWASCAT Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47. 21297633

2011
dbSNP: rs4979462
rs4979462
TNFSF15
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		T 0.830 GeneticVariation GWASCAT Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population. 23000144

2012
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		C 0.800 GeneticVariation GWASCAT Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233

2012
dbSNP: rs4979462
rs4979462
TNFSF15
CUI: C0023892
Disease: Biliary cirrhosis
Biliary cirrhosis 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population. 23000144

2012
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		T 0.800 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		G 0.800 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919

2015
dbSNP: rs7848647
rs7848647
TNFSF15
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.710 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919

2015
dbSNP: rs4366152
rs4366152
TNFSF15
CUI: C0023343
Disease: Leprosy
Leprosy 		A 0.700 GeneticVariation GWASCAT Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy. 25642632

2015
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919

2015
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs4246905
rs4246905
TNFSF15
CUI: C0033860
Disease: Psoriasis
Psoriasis 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015