Barely Significant
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Four novel candidate causal variants for deficient homozygous haplotypes in Holstein cattle.

Sci Rep · 2022 · PMC8971413 · PMID 35361830

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highly significantp = 0.0000007actually significant
It segregates within the Swiss Holstein population at an allele frequency of 5% and shows a highly significant deviation from HWE (p = 0.0000007) based on a Chi-square test (Table S6 ).

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