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Nominally significant results (P < 0.01) are cited.
Nominally significant associations were detected with several traits (Table 3).
Nominally significant; after correction for multiple testing using permutation test, all P- values > 0.10.
Only 2 families showed nominally significant effects, but chromosome-wise significance at P < 0.05 was not obtained for either family.
Of 32 independent tests across all three data sets, only 1 was nominally significant.
We found a nominally significant genotypic association with rs7633291 and allelic association with rs1025398 alleles.
Five single variants near GRB14, UBE2E2, PTPRD, VPS26A and KCNQ1 showed nominally significant interactions with PM10 (P < 0.05).
These relationships remained nominally significant even after multivariable adjustment for prognostic clinical variables.
Meta-analysis was used to combine results from the two subsets.SNPs within several interesting candidate genes were nominally significant.
Only rs9349379 in PHACTR1 achieved a nominally significant P value (P = 0.034) (Additional file 1: Table S5).
The protective effect was nominally significant in the overall population.
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