Genome-wide association (GWA) has been used to detect quantitative trait loci (QTLs) in plant and animal species. Genomic prediction is to predict an accumulative effect of all QTL effects by capturing the linkage disequilibrium between markers and QTLs. Thus, marker preselection is considered a promising method to capture Mendelian segregation effects, especially for an oligogenic trait. Using QTLs detected in the GWA study could improve genomic prediction (GP), including informative marker selection and adding a QTL with the largest effect size as a fixed effect. In this study, we performed GWA and GP studies in a population with 904 clones from 32 full-sib families planted in four trials using a newly developed 50k SNP Norway spruce array. In total, GWAS identified 41 SNPs associated with the budburst stage (BB) and the SNP with the largest effect size explained 5.1% of the phenotypic variation (PVE). For other traits like height at tree ages six and 12, diameter at breast height, frost damage and Pilodyn penetration, only 2 - 13 SNP associations were detected and the PVE of the strongest effects ranged from 1.2% to 2.0%. GP with approximately 100 preselected SNPs based on the smallest p-values from GWAS showed the largest predictive ability (PA) for the oligogenic trait BB. But for the other polygenic traits, approximate 2000-4000 preselected SNPs, indicated by the smallest Akaike information criterion (AIC) to offer the best model fit, still resulted in PA being similar to that of GP models using all markers. Analyses on both real-life and simulated data also showed that the inclusion of a large QTL SNP in the model as a fixed effect could improve the PA and accuracy of GP provided that the PVE of the QTL was >=2.5%.