A crucial component of the openSNP infrastructure is to make the available data more accessible to the general users and scientists alike. Currently, the portal has independent listing of user Phenotypes and parsed SNPs. Each SNPs entry have an additional information section where data from other credible sources (PLoS, Mendeley, Genome.gov) is made available. There is, however, no direct or inferred relationship available between the SNPs and the corresponding Phenotypes (as reported). This project proposes to bridge the connectivity between existing Phenotypes and genetic variants with the help of already mined data and implementing additional services as necessary.