Establishing causal links between inherited polymorphisms and cancer risk is challenging. Here, we focus on the single nucleotide polymorphism rs55705857 (A>G), which confers a 6-fold increased risk o
Supplementary Table S6 shows the DEPTH posterior log odds in favour of association (PLO) score and the logistic regression p-value of the lowest p-value variant for each of the 34 known glioma risk re
Supplementary Table S5 shows the generalised Berk-Jones statistic (GBJ) p-values for the candidate novel susceptibility regions for glioma by study and sex.
Previous studies have identified multiple loci for inherited susceptibility to glioma development, including the regulator of telomere elongation helicase 1 (RTEL1). However, the association between R