Barely Significant
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Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia.

Nat Commun · 2019 · PMC6803694 · PMID 31636353

Europe PMCDOI
1
hedged sentence
0.1956
closest p · 3.9× alpha
0.1956
boldest claim

The sentences

did not reach statistical significancep = 0.1956not close (p > 0.1)
The difference between SH-SY5Y(RNF170 wt ) and SH-SY5Y(RNF170 ko ) cells, however, did not reach statistical significance, (genotype*time: p = 0.1956; Fig. 3c, d ; full-factorial repeated measures analysis).

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