Barely Significant
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Whole-genome SNP association in the horse: identification of a deletion in myosin Va responsible for Lavender Foal Syndrome.

PLoS Genet · 2010 · PMC2855325 · PMID 20419149

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closest p
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The sentences

highly significantno p-value reported
These 14 highly significant SNPs encompassed a region spanning 10.5 Mb (ECA1:129228091 to 139718117).

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