Barely Significant
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Risk prediction for coronary heart disease by a genetic risk score - results from the Heinz Nixdorf Recall study.

BMC Med Genet · 2020 · PMC7487988 · PMID 32912153

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borderline significantno p-value reported
Borderline significant improvement was observed in women when comparing models consisting of established RF and CAC to established RF and genetic risk score (Δ Uno’s concordance statistics = 0.0118 ± 0.0055, p = 0.03) (Additional file: Fig. 3 (c)).

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