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

To reduce the possibility of a single disease driving the cross‐disease associations and uncover truly pleiotropic genes shared by AD and IS, we focused on shared genes that were nominally significant in each disease ( P AD < 0.05 and P IS < 0.05). 2.2.2 Meta‐analysis using Fisher's method We used Fisher's method to combine the P ‐values calculated by the VEGAS2 for each gene shared by AD and IS.
In the gene‐based analysis, four candidate genes ( CDH1 ; Transmembrane Channel like 6 ( TMC6 [MIM:605828]; NM_001127198.5 ); Eukaryotic Translation Initiation Factor 3 Subunit G ( EIF3G [MIM:603913]; NM_003755.4 ); and TRMO ) showed a nominally significant enrichment for deleterious variants in the European patients ( p CDH1 = 0.0019, p TMC6 = 0.0132, p EIF3G = 0.0133, p TRMO = 0.0399) (Table S7 ).