Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6478106
rs6478106 		0.820 GeneticVariation BEFREE CONCLUSIONS The rs6478106 T allele is associated with the risk of CD in the investigated population. 31844038

2019
dbSNP: rs6478106
rs6478106 		T 0.820 GeneticVariation GWASCAT We confirmed associations of Crohn's disease with variants in MHC (rs7765379, P = 2.11 × 10(-59)), TNFSF15 (rs6478106, P = 3.87 × 10(-45)), and STAT3 (rs9891119, P = 2.24 × 10(-14)). 23266558

2013
dbSNP: rs6478106
rs6478106 		0.820 GeneticVariation BEFREE We confirmed associations of Crohn's disease with variants in MHC (rs7765379, P = 2.11 × 10(-59)), TNFSF15 (rs6478106, P = 3.87 × 10(-45)), and STAT3 (rs9891119, P = 2.24 × 10(-14)). 23266558

2013
dbSNP: rs6478106
rs6478106 		T 0.820 GeneticVariation GWASDB We confirmed associations of Crohn's disease with variants in MHC (rs7765379, P = 2.11 × 10(-59)), TNFSF15 (rs6478106, P = 3.87 × 10(-45)), and STAT3 (rs9891119, P = 2.24 × 10(-14)). 23266558

2013
dbSNP: rs6478106
rs6478106 		0.820 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005