Human gene and disease associations for clinical-genomics and precision medicine research.
Ontology highlight
ABSTRACT: We are entering the era of personalized medicine in which an individual's genetic makeup will eventually determine how a doctor can tailor his or her therapy. Therefore, it is becoming critical to understand the genetic basis of common diseases, for example, which genes predispose and rare genetic variants contribute to diseases, and so on. Our study focuses on helping researchers, medical practitioners, and pharmacists in having a broad view of genetic variants that may be implicated in the likelihood of developing certain diseases. Our focus here is to create a comprehensive database with mobile access to all available, authentic and actionable genes, SNPs, and classified diseases and drugs collected from different clinical and genomics databases worldwide, including Ensembl, GenCode, Cl
SUBMITTER: Ahmed Z
PROVIDER: S-EPMC7240856 | biostudies-literature | 2020 Jan
REPOSITORIES: biostudies-literature
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