A probable <i>cis</i>-acting genetic modifier of Huntington disease frequent in individuals with African ancestry.

HGG Adv · 2022 · PMC9352962 · PMID 35935919

Europe PMC DOI

hedged sentence

0.0000

closest p · 0.0× alpha

0.0000

boldest claim

The sentences

highly significantp < 2 × 10 −16actually significant

The inherited expanded CAG repeat length and the age at sampling were shown to have a highly significant association with the ratio of somatic CAG expansions of the disease-associated allele observed in blood DNA (p < 2 × 10 −16 ).

also in 132,142 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.