Genetic risk variants for metabolic traits in Arab populations.

Sci Rep · 2017 · PMC5247683 · PMID 28106113

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closest p

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nominally significantno p-value reported

Markers associated with phenotype traits either at ‘close to genome-wide significant’ p-values or at ‘nominally significant’ p-values Results from tests of association pointed to only one risk variant (namely Chr15:40531386-rs12440118 from ZNF106 ) associated with HbA1c emerging at ‘close to genome-wide significant’ p-value of 3.41E-08 (with Benjamini–Hochberg FDR p-value of 0.0032) ( Table 2 ).

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