CYP1B1 rs2855658 and rs1056836 were associated with KIT exon 11 codon 557-8 del; ERCC2 rs50871 was associated with WT GIST; ERCC2 rs50871 was associated with KIT exon 11 insertion (no codon 557-8); GSTM1 deletion was associated with KIT exon 11 codon 557-8 del; RAD23B rs1805329 and rs7041137 were associated with other KIT mutations (none in exon 11). The gene discussed is ERCC2; the disease is gastrointestinal stromal tumor.