The aim of this study was to evaluate specific glutathione S-transferase (GST) gene variants as determinants of risk in patients with clear cell renal cell carcinoma (cRCC), independently or simultane
*Numbering according to the genomic sequence of CCL22 (AC003665). Position 1 is the A of the initiation codon.‡Minor allele frequencies (MAF) in the screening population (N = 12).†NCBI, number from th
Results of the multivariable logistic regression analysis of the dominant model for the A allele of RASGRF2 113808 G>A (rs26907) polymorphism in cirrhotic patients.
