Barely Significant
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“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

Despite substantial estimated heritability, only variants in the GLRA3 gene have been genome-wide significantly associated ( p -value < 5 × 10 −8 ) with diabetic albuminuria, in Finnish individuals with type 1 diabetes; However, replication attempt in non-Finnish Europeans with type 1 diabetes showed nominally significant association in the opposite direction, suggesting a population-specific effect, but simultaneously leaving the finding controversial.
3 Overall, PRS captures the cumulative effects of multiple genetic risk variants (or “genetic burden”) for a particular phenotype, and often includes thousands of independent SNPs for its calculation (in other words, it includes several SNPs that were only nominally significant in the base GWAS, in addition to the few genome-wide significant ones).
9 , 10 In a transmission disequilibrium test in Japanese families showing autism, the results of haplotype analysis, excluding the rs6265, by using the sliding window method showed nominally significant associations. 12 However, in an association study of BDNF polymorphisms in Chinese autistic patients, the frequency of the rs6265 polymorphism was not significantly different from that of the control individuals. 32 Similarly, the present study failed to identify an association between ASDs and the rs6265 polymorphism.
Nominally significant polygenic signal for the meta-analysis of unrelated AA individuals was observed based on LDSR with scores computed from 1000 Genomes African populations (z = 2.12, p = 0.017), but the quantitative estimate of h 2 g was unstable depending on the choice of reference panel, reflecting the challenge of correctly specifying LDSR and robustly modelling LD for the AA population ( Supplementary Information A11 ).