Barely Significant
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A Common Polymorphism in the <i>MTHFD1</i> Gene Is a Modulator of Risk of Congenital Heart Disease.

J Cardiovasc Dev Dis · 2022 · PMC9224796 · PMID 35735795

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marginally significantno p-value reported
Supplementary Materials The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/jcdd9060166/s1 : Table S1: Differences for all of the variables tested between the control and CHD groups using simple statistical tests and logistic regression models; Table S2: Differences in all tested variables between control and CHD etiologic sub-groups, calculated using simple statistical tests; Table S3: Statistically significant and marginally significant differences in genotypes in four most common septal (VSD & ASD), LVOTO (AS) and conotruncal (TOF) defects.

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