Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs116855232
rs116855232
0.750 GeneticVariation BEFREE Our results indicate that careful monitoring of leukopenia and dose adjustment are necessary throughout treatment in IBD patients heterozygous for the NUDT15 R139C. 31045285

2019

dbSNP: rs116855232
rs116855232
0.750 GeneticVariation GWASCAT NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. 29923122

2018

dbSNP: rs116855232
rs116855232
0.750 GeneticVariation BEFREE NUDT15 variant (rs116855232) has been recently identified as a novel polymorphism related with thiopurine-induced leucopenia in inflammatory bowel disease and ALL. 28963908

2017

dbSNP: rs116855232
rs116855232
C 0.750 GeneticVariation GWASCAT A coding variant in FTO confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBD. 27558924

2017

dbSNP: rs116855232
rs116855232
0.750 GeneticVariation BEFREE Combined detection of the 3 variants could increase the predictive sensitivity of thiopurine-induced leukopenia and help to distinguish early leukopenia in heterozygote of c.415C>T in Chinese patients with IBD. 28570428

2017

dbSNP: rs116855232
rs116855232
0.750 GeneticVariation BEFREE NUDT15 R139C-related thiopurine leukocytopenia is mediated by 6-thioguanine nucleotide-independent mechanism in Japanese patients with inflammatory bowel disease. 26590936

2016

dbSNP: rs116855232
rs116855232
0.750 GeneticVariation BEFREE NUDT R139C was significantly associated with early severe hair loss in Japanese patients with IBD. 26076924

2016