Barely Significant
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Weighted pedigree-based statistics for testing the association of rare variants.

BMC Genomics · 2012 · PMC3827928 · PMID 23176082

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may be significantno p-value reported
Taken together, these results from our analysis of FHS data support the hypothesis that the genes B4GALNT2, AKAP7 and DYRK1A may be significant for development of CVD although further molecular tests are needed to test these hypotheses although further molecular tests are warranted.

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