Variant: rs12035735 

    present in Gene: LRRC8D
    present in Chromosome: 1
    Position on Chromosome: 89839786
    Alleles of this Variant: G/A

rs12035735 in LRRC8D gene and Digestive System Disorders PMID 29923122 2018 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.

rs12035735 in LRRC8D gene and Gastrointestinal Diseases PMID 29923122 2018 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.

rs12035735 in LRRC8D gene and Inflammatory Bowel Diseases PMID 29923122 2018 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.

rs12035735 in LRRC8D gene and Intestinal Diseases PMID 29923122 2018 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.