Barely Significant
← all phrases

“nominally significant”

7,733 sentences · 7,733 papers · 10,034 search hits before verification · confirmed specimen

Sighted at

p=0.08

Listed by Hankins (2013) · Otte et al. (2022)

In the literature

In the DISCOVERY trial, genotypes of 2 SNP s in the GNAS gene were nominally significant in the prospective screening and significantly associated with VT when viewed as recessive traits in post hoc analyses ( TT vs CC / CT in c.393C>T: HR 1.42 [ CI 1.11‐1.80], P =0.005; TT vs CC / CT in c.2273C>T: HR 1.57 [ CI 1.18‐2.09], P =0.002).
R s12126142 in RA and rs6679677 in SLE were the only SNPs with nominally significant associations with ASD ( Supplementary Tables 1 and 2 ). 2) MR results There was no support for an association between RA and SLE using the IVW technique, which showed no relationship (beta=−0.077, SE=0.041, p=0.062; beta=0.014, SE=0.021, p=0.493) ( Table 1 , Figures 1 and 2 ).
SNP and Gene-Based Functional Analysis of Most Significant GWAS Hits and Their Link to Neurological Traits and Pathologies The analysis with the most nominally significant SNPs from all five linear regressions retrieved a total of 30 candidates, all with functional relevance in brain tissues, as suggested by expression and epigenetic data.
Given the large number of stratified analyses performed across multiple demographic and geographic strata, the familywise error rate is inflated and some nominally significant subgroup results may represent Type I error; accordingly, effect sizes and 95% confidence intervals are emphasized alongside p -values for subgroup comparisons, and borderline findings are interpreted with appropriate caution. 2.5.3.
6 SNPs from RRM2B and UBR5 were added to this list because they are both members of GO:6281 “DNA Repair” (which, although nominally significant in GeM, did not reach q < 0.05 and was therefore not used to create the pathway cluster), both lie within a genome‐wide significant association peak in GeM‐HD, and both have significant gene‐wide p values (see Table S5 of the GeM‐HD article). 6 For each gene, the most significant SNP was selected, along with a small number of proxy SNPs in close LD ( r 2 > 0.8) with the most significant SNP that also showed association in GeM‐HD.