Barely Significant
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Mapping causal mutations by exome sequencing in a wheat TILLING population: a tall mutant case study.

Mol Genet Genomics · 2018 · PMC5854723 · PMID 29188438

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highly significantno p-value reported
Although our initial mutation analysis revealed no obvious candidate point mutations, the highly significant association between the SNPs in the peak region on chromosome arm 4BS and the increased height phenotype suggested that the causal variant was in close proximity.

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