The 1Malaysia Human Genome Variation Consortium
Thus, it will also study the implications of the genomics database on the common diseases in Malaysia and their ethical, legal and social implications on our society.
Genomic variations in the human DNA sequences can affect the development of diseases and an individual's response to drugs, infections and vaccines. One of these genomic variations is the single nucleotide polymorphism or SNP.
In biomedical research, identification of these genomic variations will enable researchers to conduct comparative studies between matched cohorts with and without a particular disease. Discovery of these variations will provide fundamental new insights into the pathogenesis, diagnosis and treatment of human diseases and towards the development of personalized medicine.
