Barely Significant
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Genetic Variants of the <i>PLCXD3</i> Gene Are Associated with Risk of Metabolic Syndrome in the Emirati Population.

Genes (Basel) · 2020 · PMC7349663 · PMID 32570874

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nominally significantp < 0.05actually significant
As shown in Table 7 , we detected nominally significant associations ( p < 0.05) between the variant allele of PLCXD3 rs319013 with BMI, creatinine, diastolic blood pressure, eGFR-creat (serum creatinine), HbA1c, height, LDL cholesterol, pericardial adipose tissue volume, triglycerides and T2D in several datasets.

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