Exome-wide association study of blood lipids in 1,158,017 individuals from diverse populations.

Nat Genet · 2026 · PMC13263153 · PMID 42185625

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highly significantno p-value reported

Instead, we observed four independent missense variants in CELSR2 (p.Q126K, p.R2253H, p.V2287I, p.P2807A), each with highly significant associations with LDLC.

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