Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs116855232
rs116855232
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
T 0.730 GeneticVariation GWASCAT A common missense variant in NUDT15 confers susceptibility to thiopurine-induced leukopenia. 25108385

2014