Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse.
Hadji-Turdeghal K, Andreasen L, Hagen CM et al.
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Abstract
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Aims: Syncope is a common condition associated with frequent hospitalization or visits to the emergency department. Family aggregation and twin studies have shown that syncope has a heritable component. We investigated whether common genetic variants predispose to syncope and collapse.
9,163 British ancestry cases, 399,798 British ancestry controls
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