Uncovering the roles of rare variants in common disease through whole-genome sequencing
Uncovering the roles of rare variants in common disease through whole-genome sequencing
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London: Nature Publishing Group UK
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Language
English
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London: Nature Publishing Group UK
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Key Points
Genome-wide association studies of very common variants have neither identified associations that explain a large portion of the heritability for most traits studied nor identified the causal variants behind the associations seen.
Although few common variants that cause a disease have been securely identified, rare variants have be...
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Uncovering the roles of rare variants in common disease through whole-genome sequencing
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TN_cdi_proquest_miscellaneous_745726209
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_745726209
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ISSN
1471-0056
E-ISSN
1471-0064
DOI
10.1038/nrg2779
