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  • Molecular assay reagents intended to identify gene variants associated with hypercholesterolemia, a condition in which cholesterol is found at elevated levels in the blood, leading to increased risk of cardiovascular disease. Genetic variants at multiple loci have been associated with hypercholesterolemia. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple hypercholesterolemia-associated loci simultaneously.
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