Common variation at 10p12.31 near MLLT10 influences meningioma risk.
Dobbins SE, Broderick P, Melin B et al.
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Abstract
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To identify susceptibility loci for meningioma, we conducted a genome-wide association study of 859 affected individuals (cases) and 704 controls with validation in two independent sample sets totaling 774 cases and 1,764 controls. We identified a new susceptibility locus for meningioma at 10p12.31 (MLLT10, rs11012732, odds ratio = 1.46, P(combined) = 1.88 × 10(-14)). This finding advances our understanding of the genetic basis of meningioma development.
859 European ancestry cases, 704 European ancestry controls
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