SNPs- choice In genome-wide association studies on genetic causes of aging,researchers are seeking to identify genetic variations in sequences of amino acids known as:

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Genome-wide association studies typically focus on identifying single nucleotide polymorphisms (SNPs) as they are the most common type of genetic variation in the genome. SNPs can potentially influence the risk of developing a disease, including age-related conditions, by altering the function of proteins or regulatory sequences. Cytosine replacement molecules (CRM), mutation linkage abnormalities (MLA), and glycolization end-product units (GEP) are not commonly used terms in genetics or aging research.

SNPs- Choice in Genome-Wide Association Studies on Genetic Causes of Aging,researchers