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Common SNP in sequence of human genome conferring risk of vascular diseases discovered

Common SNP in sequence of human genome conferring risk of vascular diseases discovered
Scientists at deCODE genetics and academic colleagues from the Netherlands and twelve other countries across Europe and North America today report the discovery of a common single-letter variation (SNP) in the sequence of the human genome conferring risk of a range of vascular diseases. The SNP confers risk of abdominal aortic aneurysm (AAA), early-onset heart attack, peripheral artery disease …

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