Swedish population substructure revealed by genome-wide single nucleotide polymorphism data.

PLoS One · 2011 · PMC3036708 · PMID 21347369

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nominally significantno p-value reported

S9 ); while the genes closest to these SNPs showed no systematic enrichment into any Gene Ontology class, nominally significant SNPs were unexpectedly common in the MHC region and in genome areas associated to skin pigment and blood lipid traits ( Table S5 ).

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