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Single Nucleotide Polymorphisms(SNP) are the foremost common type of genetic variation in human comprising nearly1/1,000 th of the typical human genome. SNP offer the foremost complete information for genome-wide association studies. We tend to propose a process methodology to quickly notice true SNPs in public-available leukemia cancer database. Much analysis has been specializing in various genetic models to spot genes that may predict the disease status. However, increasing the amount ofdoi:10.9756/bijdm.8134 fatcat:kq7une67ebh3le5dmuqft4zwlu