I have a reasonable case control population genotyped for a panel of 20 snps related to a pathology (according to OMIM). I would like to identify the best panel of snps that allow to discriminate cases from controls. What do you think about the possibility to achieve this goal by mean of Support Vector Machines models elaborated considering all the different combinations of SNP? In other words i'm thinking to: elaborate SVM models with all the combinations of subset of SNPs estimate the accuracy of each model choose the combination of snp that provide the model(s) with the best accuracy