Validation of Polygenic Risk Scores for Coronary Heart Disease in a Middle Eastern Cohort Using Whole Genome Sequencing.

Circ Genom Precis Med · 2022 · PMC9770120 · PMID 36252120

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closest p

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nominally significantno p-value reported

Only rs1333042 ( P =0.029) was nominally significant (Figure 4 ).

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