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Detailed investigation of the role of common and low-frequency WFS1 variants in type 2 diabetes risk

Fawcett, Katherine A (author)
Wheeler, Eleanor (author)
Morris, Andrew P (author)
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Ricketts, Sally L (author)
Hallmans, Göran, 1947- (author)
Umeå universitet,Näringsforskning
Rolandsson, Olov (author)
Umeå universitet,Allmänmedicin
Daly, Allan (author)
Wasson, Jon (author)
Permutt, Alan (author)
Hattersley, Andrew T (author)
Glaser, Benjamin (author)
Franks, Paul W (author)
Umeå universitet,Medicin
McCarthy, Mark I (author)
Wareham, Nicholas J (author)
Sandhu, Manjinder S (author)
Barroso, Inês (author)
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 (creator_code:org_t)
2009-12-12
2010
English.
In: Diabetes. - : American Diabetes Association. - 0012-1797 .- 1939-327X. ; 59:3, s. 741-746
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • We identified six highly correlated SNPs that show strong and comparable associations with risk of type 2 diabetes, but further refinement of these associations will require large sample sizes (>100,000) or studies in ethnically diverse populations. Low frequency variants in WFS1 are unlikely to have a large impact on type 2 diabetes risk in white U.K. populations, highlighting the complexities of undertaking association studies with low-frequency variants identified by resequencing.

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