Barely Significant
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Genome-wide linkage analysis of congenital heart defects using MOD score analysis identifies two novel loci.

BMC Genet · 2013 · PMC3664624 · PMID 23705960

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nominally significantno p-value reported
On the other hand, on chromosome 15 a total number of 39 SNPs were found to be nominally significant and only one (rs3784481 at 99749 kb) was significant after Bonferroni correction ( P value = 0.0025).

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