Barely Significant
← all excerpts

Insights into the genetic basis of retinal detachment.

Hum Mol Genet · 2020 · PMC7068119 · PMID 31816047

Europe PMCDOI
1
hedged sentence
0.0042
closest p · 0.1× alpha
0.0042
boldest claim

The sentences

nominally significantP -value = 4.2 10 −3actually significant
The CERS2 variant rs267738 previously associated with RRD ( 16 ) shows nominally significant association, P -value = 4.2 10 −3 , with the major T allele increasing risk as previously reported.

also in 7,732 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.