Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6478108
rs6478108
0.810 GeneticVariation BEFREE Using genetic data from published studies on CD, PBC and leprosy we revealed that bearing a T allele at rs6478108/rs6478109 (r(2) = 1) or rs4979462 was significantly associated with increased risk of CD and decreased risk of leprosy, while the T allele at rs4979462 was associated with significantly increased risk of PBC. 27507062

2016

dbSNP: rs6478108
rs6478108
0.810 GeneticVariation GWASDB Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy. 22019778

2011

dbSNP: rs6478108
rs6478108
A 0.810 GeneticVariation GWASDB Genomewide association study of leprosy. 20018961

2009

dbSNP: rs6478108
rs6478108
A 0.810 GeneticVariation GWASCAT Genomewide association study of leprosy. 20018961

2009

dbSNP: rs4366152
rs4366152
A 0.700 GeneticVariation GWASCAT Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy. 25642632

2015

dbSNP: rs10114470
rs10114470
0.700 GeneticVariation GWASDB Genomewide association study of leprosy. 20018961

2009

dbSNP: rs4979462
rs4979462
0.010 GeneticVariation BEFREE Using genetic data from published studies on CD, PBC and leprosy we revealed that bearing a T allele at rs6478108/rs6478109 (r(2) = 1) or rs4979462 was significantly associated with increased risk of CD and decreased risk of leprosy, while the T allele at rs4979462 was associated with significantly increased risk of PBC. 27507062

2016

dbSNP: rs6478109
rs6478109
0.010 GeneticVariation BEFREE Using genetic data from published studies on CD, PBC and leprosy we revealed that bearing a T allele at rs6478108/rs6478109 (r(2) = 1) or rs4979462 was significantly associated with increased risk of CD and decreased risk of leprosy, while the T allele at rs4979462 was associated with significantly increased risk of PBC. 27507062

2016