Barely Significant
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Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle.

BMC Med Genomics · 2021 · PMC8502261 · PMID 34627233

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highly significantno p-value reported
Lately, a GWAS involving 4,000 unrelated Caucasian patients diagnosed with CHD indicated that ZBTB10 was associated with TGA, since two highly significant SNPs (rs148563140 and rs143638934) closely located to this gene [ 42 ].

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