Barely Significant
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Whole genome mapping and identification of single nucleotide polymorphisms of four Bangladeshi individuals and their functional significance.

BMC Res Notes · 2021 · PMC7981821 · PMID 33743798

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may be significantno p-value reported
However two of the aforementioned disease causing variants were directly associated with structural heart defects and hypercholesteremia respectively; suggesting the possibility that the variants occurring in heart function genes may be significant still.

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