Barely Significant
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MSX1 polymorphism associated with risk of oral cleft in Korea: evidence from case-parent trio and case-control studies.

Yonsei Med J · 2007 · PMC2627992 · PMID 17326252

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hedged sentence
closest p
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only marginally significantno p-value reported
All haplotype windows containing SNP7 showed significant excessive transmission of a haplotype containing the G allele, although some p-values were only marginally significant (e.g. window 4).

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