Barely Significant
← all excerpts

Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 That Confer Risk for Type 1 Diabetes.

Diabetes · 2016 · PMC4764149 · PMID 26631741

Europe PMCDOI
1
hedged sentence
0.0600
closest p · 1.2× alpha
0.0600
boldest claim

The sentences

marginally significantP = 0.06so close (0.05 < p ≤ 0.1)
The minor allele of rs74163663 co-occurred with the 1858T risk allele at rs2476601 ( Table 2 ) and showed a marginally significant association with T1D ( P = 0.06) after conditioning on rs2476601.

also in 26,082 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.