Barely Significant
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“nominally significant”

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Sighted at

p=0.08

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

In the literature

nominally significantp < 0.051.0× alphagold
After multiple testing corrections, one of these SNPs was significant (rs73349121, p = 0.0001), 9 were nominally significant ( p < 0.05, with 5 expected), and 58/99 had a direction of effect that was consistent with the Whites-only analyses (one-sided p = 0.04, Fig. 2 ).
nominally significantp < 0.051.0× alphagold
We repeated the analysis using both prevalent type 2 diabetes at baseline and incident type 2 diabetes during follow-up. We estimated the power that our study had to observe a nominally significant association ( p < 0.05) of each individual SNP or the genetic predisposition score with type 2 diabetes, based on the expected effect size (and its SE) of each individual SNP or the score on type 2 diabetes.
nominally significantP <0.051.0× alphagold
The 11bp indel in ASIP known to cause the black base coat colour was not significant ( P >0.05); however, six single nucleotide polymorphisms (SNPs) within the genomic region encoding the ASIP gene and one within MC1R were identified as being nominally significant ( P <0.05) in association with opioid analgesic effectiveness.
nominally significantp < 0.051.0× alphagold
Of the 245 UKB associations (226 previously reported + 19 previously unreported associations), we find that 72% (176) show at least nominally significant ( p < 0.05 ) age-specific effects within UK women ( Figure 2 C). 37 of these 176 associations, representing 15% of all associations, have a slope with a genome-wide significant p value ( p < 5 × 10 − 8 ), constituting a more stringent criterion (strong and moderate evidence in Figure 2C).
nominally significantP < 0.051.0× alphagold
Additionally, for each of the 594 eGFR signals, we queried further genetic association data relevant to the kidney researcher: (7) To highlight the relevance of a genetic association with creatinine-based eGFR for kidney function rather than creatinine metabolism, we included information on whether the locus association was directionally consistent and nominally significant for blood urea nitrogen (BUN) or cystatin-based eGFR (eGFRcys; i.e. locus lead variant P < 0.05; opposite or same direction of effect for BUN or eGFRcys, respectively; n = 852,678 or 460,826, respectively; yielding 491 of 594 signals validated); (8) Since genetic effects with steeper decline versus more stable eGFR over time might point to particularly deleterious mechanisms for the kidney, we included information on whether the signal showed significant association on eGFR decline (N = 343,339 [ 25 ], yielding 8 decline signals).
nominally significantp < 0.051.0× alphagold
Patients receiving etanercept monotherapy had less deterioration of PtGA and PtJP scores versus those assigned to methotrexate monotherapy, with a nominally significant treatment difference observed at almost all time points for PtGA and PtJP at weeks 12 and 36 ( p < 0.05; Fig. 1 ).
nominally significantp < 0.051.0× alphagold
Association of genetically-predicted height with clinical traits A total of 142 traits were associated with genetically-predicted height at phenome-wide significance among EA individuals, 2 of which were phenome-wide significant in AA individuals as well, and another 46 of which were nominally significant ( p < 0.05) in AA individuals ( Fig 1B and S3 and S4 Tables ).
nominally significantP <0.051.0× alphagold
Additionally, nominally significant ( P <0.05) suggestive associations with greater odds of staying at the Care Hotel were noted for younger age [OR (per 10-year increase)=0.90, P =0.035], lower Charlson comorbidity index [OR (per 1 unit increase)=0.95, P =0.032], and longer distance travelled to the hospital [OR (per each doubling)=1.09, P =0.010].