DEVELOPMENT OF TECHNIQUES FOR MUTATION DETECTION THAT MAY DISRUPT THE GENE FUNCTIONING IS OF PARAMOUNT IMPORTANCE IN MANY DISCIPLINES OF LIFE SCIENCE, PARTICULARLY IN GENETICS [1]. IN THIS POST-GENOMICS ERA WITH THE INTRODUCTION OF HIGH-THROUGHPUT TECHNOLOGIES SUCH AS NEXTGENERATION SEQUENCING THAT CAN GENERATE A FLOOD OF DATA, PRESENCE OF A FAST AND SIMPLE PROCEDURE FOR THE DETECTION OF SINGLE-NUCLEOTIDE POLYMORPHISMS (SNPS) IS LACKING. THESE GENETIC POLYMORPHISMS ARE CHARACTERIZED BY THE SUBSTITUTION OF ONE NUCLEOTIDE FOR ANOTHER AT A SPECIFIC LOCUS IN THE GENOME. SNPS HAVE BEEN USED FOR THE STUDY OF VARIOUS COMMON DISEASES AND INDIVIDUAL DIFFERENCES IN DRUG METABOLISM. [2, 3] THEREFORE, DETECTION OF SNPS IS OF PARAMOUNT IMPORTANCE IN THE DIAGNOSIS AND TREATMENT OF GENETIC DISORDERS, DRUG SCREENING AND IN FORENSIC APPLICATIONS [4]. IN THIS TALK, WE PRESENT SOME DIFFERENT PROTOCOLS INCLUDING ELECTROCHEMICAL AND ELECTROGENERATED CHEMILUMINESCENCE METHODS FOR THE genotyping OF SINGLE-NUCLEOTIDE POLYMORPHISMS [5-9].