Bioinformatics is one of the many areas which apply feature selection techniques. In bioinformatics, genome wide association studies (GWAS) is an observational study aimed at determining whether a genetic variant is associated with a certain observed trait. Single nucleotide polymorphism (SNP) is the most popular genetic marker used to identify genetic polymorphisms. Here we propose the use of variable ranking methods to remove less important SNPs prior to SNP selection. We compared methods of SNP ranking by means of statistical approaches, i.e., correlation-adjusted marginal correlation score (CAR score) and influential score (I-score), and machine learning approach using random forest algorithm in an attempt to reduce the search space. The search in the reduced space was then conducted using sequential forward floating selection (SFFS) which wraps support vector regression (SVR), and the results obtained by two of multipurpose kernels-radial basis function (RBF) kernel and Bessel kernel-were compared for this high-dimensional linear regression problem, i.e., the search for the most appropriate combination of SNPs which have association with the phenotypes of interest. We propose the use of two optimality or selection criteria, the adjusted R ! and the mean squared error, in the hope that the selected SNPs are those with both high statistical significance and strong predictive power. Testing was conducted using two simulated data sets with and without epistasis. Our results show that the intersection of the two selected subsets obtained by the two selection criteria can reduce the number of, or even eliminate, false positives. Furthermore, they suggest that the removal of less important SNPs prior to SNP selection improves the selection results. They also suggest that the proposed SNP selection method is better than the methods proposed by De Oliveira et al. (2014) and Kusuma et al. (2016).