Barely Significant
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Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences.

Intelligence · 2016 · PMC4725222 · PMID 26912939

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nominally significantno p-value reported
Regions around these index SNPs are included by adding SNPs which are nominally significant, within 250 kb and correlated (in LD of r 2 > 0.5 using the HapMap2 CEU reference panel) with the index SNP.

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