showed a trendp = 0.049
Analysis of rs12997 in PXG patients showed a trend towards association as compared to controls (Table 4 ) with G/G genotype resulting in a 2-fold increased of disease ( p = 0.049) in co-dominant model.
Analysis of rs12997 in PXG patients showed a trend towards association as compared to controls (Table 4 ) with G/G genotype resulting in a 2-fold increased of disease ( p = 0.049) in co-dominant model.
In PXG, the rs12997[G/G] genotype showed a significant trend towards increased risk of the disease (OR = 2.04, 95% CI = 0.99–4.18, p = 0.049) but did not survive the Bonferroni correction.