Single nucleotide polymorphisms: Implications in the early diagnosis and targeted intervention of coronary microvascular dysfunction.

Genes Dis · 2025 · PMC11696767 · PMID 39759113

Europe PMC DOI

hedged sentence

—

closest p

—

boldest claim

The sentences

highly significantno p-value reported

11 Therefore, the search for SNP sites is consequently highly significant for enhanced diagnosis, precise therapies, and improved prognosis of these diseases.

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.